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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

Busse Hospital Disposables, Inc.: Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable

Agency Publication Date: November 29, 2022
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Affected Products

Product: Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1

UDI-DI: (01)00849233016712 Lot Number: 2230276

Lot Numbers:
Number
Product: Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1

UDI-DI: (01) 00849233016705 Lot Number: 2230458

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91079
Status: Active
Manufacturer: Busse Hospital Disposables, Inc.
Manufactured In: United States
Units Affected: 2 products (80 cases; 40 cases)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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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.