Terminated

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FDA Recall Z-0520-2020 · Posted None

Recalling FirmZimmer Biomet, Inc.

Recall StatusTerminated

Product CodeKWS

Date Initiated2019-08-21

Date Terminated2021-07-21

Product Quantity219988 units

Reason for Recall

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

Firm Action

On September 11, 2019, the firm began notifying distributors and customers of the recall via an Urgent Medical Device Recall letter. The letter informed consignees of the product issue. Customers were asked to assist their Zimmer Biomet sales representative and quarantine all identified product. The sales representative will remove the product from your facility. If any products were further distributed, please forward the notification to responsible parties. If you have further questions or concerns, please call customer service at 574-371-3071 between 8:00 am and 5:00 pm ET, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-call representative in the event of an emergency. Alternatively, your questions may be emailed to [email protected]. There are no specific patient monitoring instructions related to this recall that are recommended beyond your existing follow-up schedule.

Root Cause

Environmental control

Distribution Pattern

US Nationwide distribution and countries of Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Ecuador, El Salvador, Italy, Netherlands, India, Japan, Korea, Malaysia, Mexico, New Zealand, Panama, Singapore, Taiwan, Thailand, Trinidad and Tobago, and Venezuela.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K172502Comprehensive Augmented Glenoid Components, Comprehensive Standard Baseplate, Comprehensive Mini BaseplateBiomet Manufacturing Corp · 2018-01-03

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.