Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalogue Number: 4894251; UDI/DI: 04022495101167; Lot/Batch: 20E15, 19L09, 19L27, 20A19, 20H21, 21G14, 21I16, 22H23,
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- B Braun Medical Inc
- Reason for Recall:
- The devices are labeled "not made with DEHP" or the DEHP free symbol; however, the glue used contains traces of DEHP.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Stimuplex A, 30 DEG, 24GX1", 0.55x25mm, Catalogue Number: 4894251.
Product Codes/Lot Numbers:
Catalogue Number: 4894251; UDI/DI: 04022495101167; Lot/Batch: 20E15, 19L09, 19L27, 20A19, 20H21, 21G14, 21I16, 22H23,
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2131-2024
Related Recalls
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).
Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).