Reported May 6, 2026 · Ongoing

Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:…

Zimmer, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zimmer, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304

Is this the product you have?

  • Brand NameDisposable
  • Mixing Bowls with Spatula Product NameMixing
  • Bowl and Spatula Model/Catalog Number00-5049-011-00
  • Software VersionN/A
  • Product DescriptionMixing
  • Bowl and Spatula ComponentN/A
Lot codes and dates

40 of 40 products

Products covered by this recall
Model / numberBarcodesProduct as published
00504901100Lot Code
0088902437971820-Pack UDI (01)00889024379718(17)301014(10)85390029
00889024376564Individual UDI (01)00889024376564(17)301014(10)85390029
00504901100Lot Number 85390029
0088902437971820-Pack UDI (01)00889024379718(17)301103(10)85682882
00889024376564Individual UDI (01)00889024376564(17)301103(10)85682882
00504901100Lot Number 85682882
0088902437971820-Pack UDI (01)00889024379718(17)301001(10)85390028
00889024376564Individual UDI (01)00889024376564(17)301001(10)85390028
00504901100Lot Number 85390028
0088902437971820-Pack UDI (01)00889024379718(17)300422(10)82395239
00889024376564Individual UDI (01)00889024376564(17)300422(10)82395239
00504901100Lot Number 82395239
0088902437971820-Pack UDI (01)00889024379718(17)300423(10)82395240
00889024376564Individual UDI (01)00889024376564(17)300423(10)82395240
00504901100Lot Number 82395240
0088902437971820-Pack UDI (01)00889024379718(17)300929(10)85390027
00889024376564Individual UDI (01)00889024376564(17)300929(10)85390027
00504901100Lot Number 85390027
0088902437971820-Pack UDI (01)00889024379718(17)300924(10)85390026
Amount recalled
66960

Where it was sold

Why it was recalled

Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised sterile barrier may lead to clinically insignificant extension of surgery or infection leading to surgical intervention.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:16 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.