Reported May 19, 2021 · Terminated
Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420
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?
- KitCentralLineDresChangeClrSeq
- MAI Kit Part Number79420
- Lot codes and dates
- Kit Number79420
- UDI (GTIN)20809160247775
- Lot Number0000276767 (Expiration
- Date
01/31/2022)0000278361 (Expiration
- Date05/31/2022)
- and 0000281458 (Expiration Date08/31/2022)
- Amount recalled
- 30 cases (20 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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