🔍 RecallPedia

B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)

Class I - Dangerous
🏥 Medical Devices Recalled: September 15, 2022 Medical Action Industries, Inc. 306 Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 10809160283875, Batch/Lot number 298442
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Medical Action Industries, Inc. 306
Reason for Recall:
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)

Product Codes/Lot Numbers:

UDI/DI 10809160283875, Batch/Lot number 298442

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0265-2023

Related Recalls

Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250 each/case), 6141 (250 each/case), 6203 (40 each/case), 6805 (50 each/case), 6805-1 (175 each/case), 6810 (50 each/case), 6810-1 (350 each/case), 6830 (8 rolls/case), and 6860 (8 rolls/case)

Medical Action Industries, Inc. 306

Class I - Dangerous

The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN.

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