BD Microtainer Quikheel Lancet 1 — Class II medical device recall Z-2192-2013
Terminated recall by Becton Dickinson & Company, reported 2013-09-18, distributed in CT, IL, KY, NY, PA, TX, VA. The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
| Recall number | Z-2192-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2013-07-10 |
| Classified | 2013-09-11 |
| Reported by FDA | 2013-09-18 |
| Terminated | 2014-03-19 |
| Distributed | CT, IL, KY, NY, PA, TX, VA |
| Countries outside the US | CA |
| Lot numbers | 3116007 |
| Model numbers | 368101 |
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 for recall
The Lancet will not retract after activation thus creating a potential for exposure to a used sharp.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2192-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.