McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
FDA device recall Z-2940-2024 · posted 2024-08-29 · Open, Classified
Recall details
- Recalling firm
- Cypress Medical Products LLC
- Reason for recall
- Affected syringes lack FDA clearance.
- Action taken
- On July 24, 2024, the firm issued Urgent Medical Device Recall letters to affected customers. Consignees were advised that the affected syringes lack FDA clearance. Customers should immediately quarantine and discontinue use of any affected product. Recalled product should be destroyed on location. If you have further distributed the product, please notify your downstream accounts of the recall. For questions about this notification please contact productcomplaint@McKesson.com.
- Root cause
- Other
- Status
- Open, Classified
- Product code
- FMF
- Quantity affected
- 24,693,200 eaches (US)
- Distribution
- US distribution only. Domestic distribution nationwide.
- Date initiated
- 2024-07-24
- Date posted
- 2024-08-29
- Location
- Richmond, VA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| JIANGSU SHENLI MEDICAL PRODUCTION CO. LTD. PISTON SYRINGE (5CC LUER LOCK) (K103830) | Jiangsu Shenli Medical Production Factory | 2011-07-29 |