MEDLINE INDUSTRIES, LP - Northfield: Medline Convenience kits labeled as: 1) SH STRL UMBILICAL ACC PACK-LF, Pack Number DYNJ0621408V; 2) SH STRL UMBILICAL ACC PACK-LF, Pack Number DYNJ0621408VH; 3) 6" ACE BANDAGE PACK-LF, Pack Number DYNJ0864492A ; 4
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality
Product Recall
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MEDLINE INDUSTRIES, LP - Northfield: Medline convenience kits labeled as: 1) PERMANENT PACING, Pack Number 00-400361J ; 2) NORTON CHILDRENS CATH LAB-LF, Pack Number 00-401185Q ; 3) PACEMAKER TRAY, Pack Number 00-401521F ; 4) FEMORAL PACK, Pack Number
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: XXX. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Distribution: Worldwide distribution.. Classification (Class II — potential health risk).
Product Recall
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Baxter Healthcare Corporation: Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits labeled as: 1. WELCH ALLYN 2-Piece Reusable Blood Pressure Cuff Kits, Product Code/Part Numbers: 2. WELCH ALLYN Reusable Blood Pressure Cuff Kit, Product Code/Part N
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.. Recalled by Baxter Healthcare Co…
Product Recall
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Baxter Healthcare Corporation: Hillrom Welch Allyn Diagnostic Cardiology Suite (formerly Connex Cardio); Diagnostic spirometer
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture…
Product Recall
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Baxter Healthcare Corporation: Welch Allyn DuraShock Aneroid Gauge Sets with a Reusable Blood Pressure Cuff labeled as: 1) WELCH ALLYN DURASHOCK Aneroid Gauge Sets with a Reusable Blood Pressure Cuff, Product Code Part Numbers: 5098-02, 5098-23, 5098
FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Recall reason: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.. Recalled by Baxter Healthcare Co…
Product Recall
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