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Product Recalls & Refunds Online / National

Becton Dickinson Infusion Therapy Systems Inc.: BD Nexiva, 20 GA 1.00 IN (1.1 X

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: There is a breach in the product packaging that renders the product non-sterile.. Recalled by Becton Dickinson Infusion Therapy Systems Inc.. Distribution: U.S. Nationwide Distribution: AR, AZ, MA, GA, NC, OH, WA, NY, NJ, HI, CA, MD, RI, MT, IN, PA, IL OK, OR, AK, CT, TX, ME, MO, FL, VA, LA, CO, UT O.U.S.: None. Classification (Class II — potential health risk). Affected lots/dates: Catalog number/Model number: 383536; Batch numbers/UDI numbers: Lot: 1193055/(17)240630(10)1193055(30)80/(01)50382903835. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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