Well Leg Holder With Boot, part of the Supine Universal Hip Distractor System; Ref (Part) #72200632; Manufactured for Sm
FDA device recall Z-0872-2007 · posted 2007-06-06 · Terminated
Recall details
- Recalling firm
- Smith & Nephew, Inc Endoscopy Division
- Reason for recall
- The device was not manufactured to correct specification causing interference when used in conjunction with Patient Transfer Board.
- Action taken
- Firm notified consignees by letter and phone call on 11/1/2006. Consignees asked to return out-of-spec Well Leg Holder for a replacement.
- Root cause
- Other
- Status
- Terminated
- Product code
- NBH
- Quantity affected
- 12
- Distribution
- Nationwide Distribution: USA including states of WI, CA, MO, IL, TX, MA, WA, NM, FL, NH, and SC and the UK
- Date initiated
- 2006-11-01
- Date posted
- 2007-06-06
- Date terminated
- 2008-06-16
- Location
- Oklahoma City, OK
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