# FDA recall Z-0325-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-10-10.

## Product

Various Knee Systems, Item Nos. 32855411838  32855411840  32855411842  32855411843  32855420307  32855420308  32855420309  32855420310  32855420315  32855430491  32855430497  32855430499  32855430500  32855430502  32855430503  32855430511  32855430526  32855430530  32855430531  32855430536  32855430537  32855430538  32855430539  32855430541  32855430543  32855430546  32855430548  32855430549  32855430550  32855430551  32855430556  32855430557  32855430558  32855430563  32855430565  32855430567  32855430568  32855430569  32855430570  32855430574  32855430575  32855430577  32855450420  32855450441  32855450453  32855450461  32855450499  32855470626  32855470639  32855470641  32855470644  32855470645  32855470648  32855470649  32855470652  32855470653  32855470654  32855470660  32855470663  32855470666  32855470667  32855470669  32855470672  32855470673  32855470679  32855470680  32855470682  32855470683  32855470684  32855470686  32855470688  32855470689  32855470692  32855470693  328554

## Reason for recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0325-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-10
- **Report date:** 2019-11-13
- **Termination date:** 2020-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0325-2020

## Citation

> AI Analytics. FDA recall Z-0325-2020. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0325-2020. Source: US FDA. Licensed CC0.

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