FDA Device recall Z-2192-2013
BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lake…
- FDA Device
- Class II
- terminated
- Published 2013-09-18
On 2013-09-18 the FDA classified a Class II recall of BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lake… by Becton Dickinson And, citing the Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2192-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-10 |
| Published | 2013-09-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Becton Dickinson And |
| Distribution | CT, IL, KY, NY, PA, TX, VA |
Product
BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417 USA Made in USA. Used to perform heel sticks for the purpose of collecting skin puncture blood.
Reason
The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
Identifiers
| code_info | REF # 368101 Lot #3116007 Class I Exempt Device listing Number E158602 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2192-2013%22
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