Quick Facts at a Glance
- Recall Date
- April 28, 2026
- Hazard Level
- HIGH
- Brand
- Mentor Texas LP
- Geographic Scope
- 3 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Mentor Texas LP
- Model numbers
- 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
- Where affected
- CA, FL, PA
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
April 28, 2026
Reported by FDA DEVICE
July 8, 2026
RecallRadar source check
July 14, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
A single lot of expired syringes were distributed due to a distribution system control failure.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Mentor Texas LP or your healthcare provider for instructions. Notification method: Letter
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Full Description
SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston. Reason: A single lot of expired syringes were distributed due to a distribution system control failure.. Classification: Class II. Quantity: 1401 syringes. Distribution: U.S.: CA, FL, and PA
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: How to Get Refunds and ReplacementsWant to Know First?
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