FDAFDA recall Z-2614-2026 · Jul 8, 2026
Mentor Texas LP: SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe recall
Recall found
Product
SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston
Reason for recall
A single lot of expired syringes were distributed due to a distribution system control failure.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- BD Product Code: 302995 Mentor Product Code: B9604 Sales Unit Box UDI-DI/GTIN code: 30382903029952 Individual Unit UDI-DI/GTIN code: 00382903029952 Lot Number: 8298877
- Quantity
- 1401 syringes
- Distribution
- U.S.: CA, FL, and PA
- Recalling firm
- Mentor Texas LP, Coppell, TX
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-04-28
Source: openFDA enforcement record Z-2614-2026 · search recall number Z-2614-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.