Reported Dec 18, 2013 · Terminated
Product is labeled in part: LIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China;…
Hospira Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- Product is labeled in partLIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China; Hospira, Inc.,; Lake Forest, IL 60045 USA. Used to isolate suction waste during surgeries, or to clear patient airways, throat or wounds to allow treatment
- Lot codes and dates
- *** DOMESTIC PRODUCT ***
- List Numbers43449-04-11 and 43449-04-01
- Lot NumbersAll; *** FOREIGN PRODUCT ***
- List Numbers
0L21297W10L21297010L213970143449001L4344901014344901024344901814344901814344901824344901DX4344961014344961614344961A1434499090
- LotsAll
- Amount recalled
- 3,560 units distributed from June 2004 - December 2012
Where it was sold
Why it was recalled
Hospira has recieved reports that the vacuum needed to create suction with the 1L Receptal System cannot be achieved due to the canister and liner not properly seating.
This product could cause temporary or reversible health problems — stop using it.
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