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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

MEDLINE INDUSTRIES, LP - Northfield: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.

Agency Publication Date: October 21, 2022
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Affected Products

Product: MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245

UDI/DI: (01)40889942604723 (case), (01)10889942604722 (kit),Lot Number 22FMF306

Lot Numbers:
Number
Product: MEDLINE PHERIPHERAL BLOOD CULTURE DRAW, Reorder #: DYNDH1561

UDI/DI: (01)40193489402811 (case), (01)10193489402810 (kit), Lot Number 22FMF307

Lot Numbers:
Number
Product: MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592

UDI/DI (01)40193489497220 (case), (01)10193489497229 (kit), Lot Numbers: 22GME974, 22FMF309

Lot Numbers:
Numbers
Product: MEDLINE 24 BLOOD CLUTURE KIT, Reorder #: DYNDH1632

UDI/DI: (01)40193489916141 (case), (01)10193489916140 (kit), Lot Number: 22FMF305

Lot Numbers:
Number
Product: MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756

UDI/DI: (01)40888277983824 (case), (01)10888277983823 (kit), Lot Numbers: 22EMI516, 22DMG491

Lot Numbers:
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90911
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Manufactured In: United States
Units Affected: 5 products (900 kits; 1020 kits; 1600 kits; 760 kits; 460 kits)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.