Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD — Class II medical device recall Z-0564-2013
Terminated recall by Becton Dickinson & Company, reported 2012-12-26, distributed nationwide. BD received a complaint report for mixed syringe tips (oral and non-oral syringe tips) within the same lot.
| Recall number | Z-0564-2013 |
|---|---|
| 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 | 2012-10-02 |
| Classified | 2012-12-19 |
| Reported by FDA | 2012-12-26 |
| Terminated | 2016-05-03 |
| Distributed | Nationwide (US) |
| Quantity | 2,786,000 units |
| Lot numbers | 1346419, 2020056, 2020057, 2055156, 2076404, 305217, 305219 |
| Model numbers | 1346419, 2020056, 2020057, 2055156, 2076404, 305217, 305219 |
Product
Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD, Franklin Lakes, NJ 07417 USA Made in USA www.bd.com BD, Laagstraat 57, B-9140 Temse, Belgium On 100 unit plastic bag: BD oral syringes are intended to dispense oral medications.
Reason for recall
BD received a complaint report for mixed syringe tips (oral and non-oral syringe tips) within the same lot.
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-0564-2013. 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.