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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
Medical Devices/Surgical Equipment

Disposable Mixing Bowls and Spatulas Recalled for Defective Package Seals

Agency Publication Date: April 24, 2026
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Summary

Zimmer, Inc. is recalling approximately 66,960 Disposable Mixing Bowls with Spatulas because the package seals may be defective. The company received ten complaints of incomplete seals, wrinkles, or peeling, which can compromise the sterile barrier required for surgery. These kits were sold nationwide and internationally through hospital suppliers and medical device distributors.

Risk

A compromised sterile barrier can lead to surgical infections or cause delays during an operation if the defect is discovered mid-procedure, potentially requiring additional surgical intervention.

What You Should Do

  1. Check your inventory for Disposable Mixing Bowls with Spatula (Model/Catalog Number 00-5049-011-00).
  2. Look for lot numbers 85390029, 85682882, 85390028, 82395239, 82395240, 85390027, 85390026, 82395238, 85390025, 85390022, 85390024, 85390023, or 86970970.
  3. See the Affected Products section below for the full list of affected codes.
  4. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  5. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Disposable Mixing Bowls with Spatula
Model / REF:
00-5049-011-00
Lot Numbers:
85390029
85682882
85390028
82395239
82395240
85390027
85390026
82395238
85390025
85390022
85390024
85390023
86970970
UDI:
00889024379718
00889024376564

Affected units include both 20-pack UDIs and individual UDIs across the listed lot numbers.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98665
Status: Active
Manufacturer: Zimmer, Inc.
Sold By: Hospital suppliers; Medical device distributors
Manufactured In: United States
Units Affected: 66,960
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Michigan, Missouri, Mississippi, North Carolina, Nebraska, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Washington, Wisconsin

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.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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 ยท 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.