BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Com
FDA device recall Z-2192-2013 · posted 2013-09-11 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
- Action taken
- BD notified their customers and distributors by phone, e-mail, and/or letter/notice of return/ customer packing list on 7/10/2013.
- Root cause
- Component change control
- Status
- Terminated
- Product code
- FMK
- Quantity affected
- US - 39,800 units ; Canada - 18,400 units
- Distribution
- Distributed in the states of CT, KY, IL, NY, PA, TX, and VA and the country of Canada.
- Date initiated
- 2013-07-10
- Date posted
- 2013-09-11
- Date terminated
- 2014-03-19
- Location
- Franklin Lakes, NJ
Monitor recalls programmatically
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