Public recall detail

Mixing Bowl And Spatula, 20- Pack

2026-04-14

medium
Orthopaedics Sterility
Quick summary

Quick summary: Mixing Bowl And Spatula, 20- Pack. Reason: Sterility. Category: Orthopaedics. Date: 2026-04-14.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Mixing Bowl And Spatula, 20- Pack. Reason: Sterility. Category: Orthopaedics. Date: 2026-04-14.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandZimmer Inc.
ProductMixing Bowl And Spatula, 20- Pack
IssueMedical devices - Sterility
Recall classType II
IdentificationRA-81888

Affected products

ProductMixing Bowl And Spatula, 20- Pack
Lot85390028
Model00-5049-011-00
Serial number85390028
DescriptionMixing Bowl And Spatula, 20- Pack
ProductMixing Bowl And Spatula, 20- Pack
Lot82395238
Model00-5049-011-00
Serial number82395238
DescriptionMixing Bowl And Spatula, 20- Pack
ProductMixing Bowl And Spatula, 20- Pack
Lot85390022
Model00-5049-011-00
Serial number85390022
DescriptionMixing Bowl And Spatula, 20- Pack
ProductMixing Bowl And Spatula, 20- Pack
Lot85390024
Model00-5049-011-00
Serial number85390024
DescriptionMixing Bowl And Spatula, 20- Pack

Issue

Zimmer Biomet is conducting a lot specific medical device recall removal for the mixing bowl and spatula. 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. Seal integrity testing conducted internally showed potential sterility breach in 7.5% of the tested units that had visual seal nonconformities. The devices are distributed in 20-pack boxes. The defectiveness was discovered on November 19, 2025. Issue was identified through the complaints handling process.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Orthopaedics
CompaniesZimmer Inc. 1800 West Center Street, Warsaw, Indiana, United States, 46580
Recall date2026-04-02
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81888
Background{}
CompaniesZimmer Inc. 1800 West Center Street, Warsaw, Indiana, United States, 46580
AudiencesHealthcare
Source updated2026-04-14

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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