Golden State Medical Supply Inc.: GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, Manufactured by Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett, Inc., Seymour, IN 47274, Packaged by GSMS Incorpora
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolutio…
Product Recall
CA
Medtronic Inc.: Medtronic, REF: MMT-7008D, Enlite Glucose Sensor for the following packaging: ENLITE AUS 1 PRESS 1PK; GTIN: 00763000252045 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously mon
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020C1 Guardian Sensor (3) for the following packaging: GS3 5PK OUS1/ GTIN: 20643169704071 GS3 5PK 9L OUS1/ GTIN: 20763000243320 GS3 5PK 9L OUS1/ GTIN: 20763000318844 Product Usage: intended for use with Medtronic D
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7008B, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 23L 1CL / GTIN: 00643169541719 ENLITE PLUS 2L 1CL PR/ GTIN: 00643169786738 ENLITE PLUS 1PK 23L 1CL/ GTIN: 00763000421304 Product Usage: intended
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic, REF: MMT-7008A, Enlite Glucose Sensor for the following packaging: ENLITE PLUS 5PK 23L 1CL /GTIN: 20643169541706, ENLT PLUS 5PK 2L 1CL PR/ GTIN: 20643169786725, ENLITE PLUS 5PK 23L 1CL/ GTIN: 20763000421292 - Product Usage:
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated s…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020C2 Guardian Sensor (3) for the following packaging: GS3 5PK 9L OUS2/ GTIN: 20763000243344 GS3 5PK 9L OUS2/ GTIN: 20763000318868 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020C5 Guardian Sensor (3) for the following packaging: GS3 5PK 1L AUS/ GTIN: 20763000252056 GS3 5PK 1L AUS/ GTIN: 20763000414362 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing s
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020D5 Guardian Sensor (3) for the following packaging: GS3 1PK 1L AUS/ GTIN 00763000252069 GS3 1PK 1L AUS/ GTIN 00763000414375 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing sys
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020LA, Guardian Sensor (3) for the following packaging: GS3 5PK US/ GTIN: 20763000336985 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose l
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020C4 Guardian Sensor (3) for the following packaging: GS3 5PK 2L CANADA/ GTIN: 20763000179612 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glu
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020LB, Guardian Sensor (3) for the following packaging: GS3 1PK US/ GTIN: 763000336998 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucose lev
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020GA, Guardian Sensor (3) for the following packaging: GS3 5PK US GC/ GTIN: 20763000179629 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor glucos
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020D4 Guardian Sensor (3) for the following packaging: GS3 1PK 2L CANADA/ GTIN: 00763000179595¿ Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously monitor gl
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic, REF: MMT-7008C, Enlite Glucose Sensor for the following packaging: ENLITE AUS 1 PRESS 5PK/ GTIN: 20763000252032 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing systems to continuously mon
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020D3 Guardian Sensor (3) for the following packaging: GS3 1 PK OUS3/ GTIN: 00643169704121 GS3 1PK 9L OUS3/ GTIN: 00763000318895 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing s
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020D1 Guardian Sensor (3) for the following packaging: GS3 1PK OUS1/ GTIN: 00643169704084 GS3 1PK 9L OUS1/ GTIN: 00763000243333 GS3 1PK 9L OUS1/ GTIN: 00763000318857 Product Usage: intended for use with Medtronic D
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020A, Guardian Sensor (3) for the following packaging: GS3 5PK 2L US/ GTIN: 20763000140940 GS3 5PK 2L US/ GTIN: 20763000337005 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing sys
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020C3 Guardian Sensor (3) for the following packaging: GS3 5PK OUS3/ GTIN: 20643169704118 GS3 5PK 9L OUS3/ GTIN: 20763000243368 GS3 5PK 9L OUS3/ GTIN: 20763000318882 Product Usage: intended for use with Medtronic D
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020D2 Guardian Sensor (3) for the following packaging: GS3 1PK 9L OUS2/ GTIN: 00763000243357 GS3 1PK 9L OUS2/ GTIN: 00763000318871 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020B, Guardian Sensor (3) for the following packaging: GS3 1PK 2L US/GTIN: 00763000140779 GS3 1PK 2L US/ GTIN: 00763000337049 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose sensing syst
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
Medtronic Inc.: Medtronic REF: MMT-7020C Guardian Sensor (3) kit for the following packaging: GS3 SEMI 5PK OUS/ GTIN: 20763000192086, 5PK SF NEW GS3 OUS/GTIN: 20763000358451 Product Usage: intended for use with Medtronic Diabetes (Medtronic) glucose
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Use of the continuous glucose monitoring system while actively taking hydroxyurea, an anti-neoplastic drug could result in inaccurate elevated…
Product Recall
CA
123Herbals: Vail-Bon Jie Yang Wan capsules, 30-count bottle, Vall Boon Medical Factory Sdn. Bhd., No 1, Lorong Mengkudu, Taman Mengkudu, 14100 Juru, Malaysia.
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared dexamethasone and chlorpheniramine.. Recalled by 123Herbals. D…
Product Recall
CA
Private Label Partners, Inc.: Selenium Sulfide 2.25% Shampoo, 180mL bottle, Rx Only, Manufactured for: Bi-Coastal Pharma Int. LLC, Shrewsbury, NJ 07702, NDC 42582-900-06.
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: CGMP Deviations: Stability data does not support expiry date.. Recalled by Private Label Partners, Inc.. Distribution: NJ. Classification (Class
Product Recall
CA
Nubratori, Inc: Dexonto 0.4% (dexamethasone sodium phosphate) solution 20 mg/5 mL (4 mg/mL), Rx Only, 12 - 5 mL Single Dose Units per box, Preservative Free, For Iontophoresis Use Only, Non-Sterile Product, Not for Injection, NUBRATORI RX, 381 Van Ne
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Labeling: Incorrect or Missing Lot and/or Expiration date: Individual vials of Dexonto 0.4%, are labeled correctly with the BUD of 12/25/2024, ho…
Product Recall
CA
Preferred Pharmaceuticals, Inc.: Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by Preferred Pharmaceuticals NDC 68788-8666-01
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and
Product Recall
CA
Generitech Corporation: 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1 fl. oz., 30 mL Bottle, For Professional Use Only, Only YourRx Inc., Chatsworth, CA 91311, Made in USA, Onlyyourrx.com.
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: CGMP Deviations: Inconsistency in the water systems.. Recalled by Generitech Corporation. Distribution: CA. Classification (Class II — potential
Product Recall
CA
Preferred Pharmaceuticals, Inc.: Ibuprofen Tablets, USP 400mg, Generic for Motrin, Pkg Size: 30 tablets per bottle, Mfg: Dr. Reddy's Laboratories, Louisiana, Shreveport, NDC 68788-9110-03.
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Failed Impurities/Degradation Specifications - at 18-month Stability testing. Recalled by Preferred Pharmaceuticals, Inc.. Distribution: CA and N…
Product Recall
CA
Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles: PERIPHERAL PARENTERAL NUTRITION, Compounded Sterile Preparation, Refrigerated Injection, Rx Only, Single Dose Injection, a) 1440 mL bag, b) 1700 mL bag, Central Admixture Pharmacy Services
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficient…
Product Recall
CA
Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles: TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Los Angeles, 1
FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price
Recall reason: Incorrect Product Formulation: product did not contain insulin as listed in the label.. Recalled by Central Admixture Pharmacy Services, Inc (CAP…
Product Recall
CA
The Bonami Baking Company, Inc.: Whole Grain Par Baked Jalapeno Cheddar Bagel --- Ingredient Declaration: Whole White Wheat Flour, Enriched Flour (Unbleached Wheat Flour, Malted Barley Flour, Niacin, Iron, Thiamine Mononitrate (Vitamin B1), Riboflavi
FDA food recall — return recalled product to store for a full refund of purchase price
Recall reason: Undeclared milk from Contains statement.. Recalled by The Bonami Baking Company, Inc.. Distribution: CA. Classification (Class II — potential hea…
Product Recall
CA