Reported May 19, 2021 · Terminated
Kit: Midline Insertion DA. MAI Kit Part Number: 77981B
Medical Action Industries, Inc. 306
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medical Action Industries, Inc. 306 · 25 Heywood Rd · Arden, NC · 28704-9302
Is this the product you have?
- KitMidline Insertion DA
- MAI Kit Part Number77981B
- Lot codes and dates
- Kit Number77981B
- UDI (GTIN)20809160284053
- Lot Number0000281502 (Expiration
- Date
04/08/2022)0000282039 (Expiration
- Date
04/08/2022)0000274390 (Expiration
- Date07/09/2021)
- and 0000279101 (Expiration Date11/13/2021)
- Amount recalled
- 110 cases (5 kits per case)
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Stop using this product now
Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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