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

    • 10097012
    • 10281012
    • 11087012
    • 11178012
    • 12066012
    • 12335012
    • 13234012
    • 14178012
    • 10105012
    • 10298012
    • 11095012
    • 11189012
    • 12101012
    • 12348012
    • 13248012
    • 14197012
    • 10130012
    • 10312012
    • 11105012
    • 11206012
    • 12108012
    • 12353012
    • 13263012
    • 14254012
    • 10162012
    • 10322012
    • 11115012
    • 11229012
    • 12138012
    • 13046012
    • 13302012
    • 14260012
    • 10172012
    • 10337012
    • 11130012
    • 11269012
    • 12156012
    • 13086012
    • 13319012
    • 10195012
    • 10340012
    • 11139012
    • 11313012
    • 12159012
    • 13095012
    • 14029012
    • 10205012
    • 11003012
    • 11146012
    • 11337012
    • 12199012
    • 13108012
    • 14052012
    • 10238012
    • 11013012
    • 11147012
    • 12016012
    • 12248012
    • 13143012
    • 14058012
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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 31, 2015 · Data as of Sep 19, 5:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.