Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    1) REF DYNJ39461J, UDI/DI 10195327112721 (EA) 40195327112722 (CS), Lot Numbers: 22BBZ954, 22FBB472, 22GBS127, 22HBJ021, 22IBN757, 22LBN387, 22LBP618, 23BBL804, 23FBL965, 23HBG346, 23IBV491, 23JBW568, 24ABJ924, 24CBG585, 24DBM211, 24FBN899, 24FBQ913, 24HBL252, 24HBV561; 2) REF DYNJ80200B, UDI/DI 10195327213978 (EA) 40195327213979 (CS), Lot Numbers: 22HBG124, 22IBJ978, 22JBL067, 22LBQ534, 23ABM279, 23BBR168, 23DBB055, 23EBV555, 23GBB476, 23IBF093, 23KBT109, 24ABA171, 24CBB183, 24DBM493, 24GBB326, 24HBB911.
  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:
MEDLINE INDUSTRIES, LP - Northfield
Reason for Recall:
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.

Product Codes/Lot Numbers:

1) REF DYNJ39461J, UDI/DI 10195327112721 (EA) 40195327112722 (CS), Lot Numbers: 22BBZ954, 22FBB472, 22GBS127, 22HBJ021, 22IBN757, 22LBN387, 22LBP618, 23BBL804, 23FBL965, 23HBG346, 23IBV491, 23JBW568, 24ABJ924, 24CBG585, 24DBM211, 24FBN899, 24FBQ913, 24HBL252, 24HBV561; 2) REF DYNJ80200B, UDI/DI 10195327213978 (EA) 40195327213979 (CS), Lot Numbers: 22HBG124, 22IBJ978, 22JBL067, 22LBQ534, 23ABM279, 23BBR168, 23DBB055, 23EBV555, 23GBB476, 23IBF093, 23KBT109, 24ABA171, 24CBB183, 24DBM493, 24GBB326, 24HBB911.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0787-2025

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