Reported May 13, 2015 · Terminated
Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main components: the suction reservoir, the PVC…
Stryker Instruments Div. of Stryker Corporation
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: Stryker Instruments Div. of Stryker Corporation · 4100 E Milham Ave · Portage, MI · 49002-9704
Is this the product you have?
- Ambulating Bulb Ambulating BulbThe Ambulating
- Bulb comprises four main componentsthe suction reservoir, the PVC tubing, the slide clamp and the female connector. The rigid polycarbonate female connector is used to connect the ambulating bulb to the CBCII evacuator tube in order to collect wound drainage
- Lot codes and dates
- Part Number0225-028-852
- and lot numbers
74 of 74 codes
100970121028101211087012111780121206601212335012132340121417801210105012102980121109501211189012121010121234801213248012141970121013001210312012111050121120601212108012123530121326301214254012101620121032201211115012112290121213801213046012133020121426001210172012103370121113001211269012121560121308601213319012101950121034001211139012113130121215901213095012140290121020501211003012111460121133701212199012131080121405201210238012110130121114701212016012122480121314301214058012
- Amount recalled
- 2,575 boxes (25,750 each)
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
- Nationwide
Why it was recalled
Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulating Bulb for a potential sterility breach in the packaging
This product could cause temporary or reversible health problems — stop using it.
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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