Bedside PICC CDS Convenience Kit
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model #: CDS984642 Lot #: 19JBB553 UDI: GTIN (01)40884389882825 EXP (17)2021-09-30 LOT (10)19JBB553
- 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:
- Medline Industries Inc
- Reason for Recall:
- NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Bedside PICC CDS Convenience Kit
Product Codes/Lot Numbers:
Model #: CDS984642 Lot #: 19JBB553 UDI: GTIN (01)40884389882825 EXP (17)2021-09-30 LOT (10)19JBB553
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0362-2022
Related Recalls
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.