NIPRO Safe Touch Safety Scalp Vein Set
Class I - DangerousWhat Should You Do?
- Check if you have this product: Product Code: PR+25G19, Lots #s 12H31H and 12I14H; Product Code: SPR+21G19, Lots #s 12I24 and 12J11; Product Code: PR-25G19, Lot # 12H27H; and PR-23G19, Lot # 12I12H.
- 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:
- Nipro Medical Corporation
- Reason for Recall:
- There is a possibility of a crack in the CP luer connector. The position of the crack is at the connection site of the CP luer connector and the tubing. The crack could cause or contribute to leakage of fluids.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
NIPRO Safe Touch Safety Scalp Vein Set
Product Codes/Lot Numbers:
Product Code: PR+25G19, Lots #s 12H31H and 12I14H; Product Code: SPR+21G19, Lots #s 12I24 and 12J11; Product Code: PR-25G19, Lot # 12H27H; and PR-23G19, Lot # 12I12H.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1834-2014
Related Recalls
Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Nipro Medical
Class I - Dangerous
Screw may loosen or fallout of Hemodialysis system
There is a possibility of the heparin line is occluded.
Class I - Dangerous
Blood foaming was found during evaluation of the product.