Data Foundry

Medical device recalls 2016

Zimmer Periarticular Locking Plate System 3 — Class II medical device recall Z-0646-2016

Terminated recall by Zimmer Biomet, Inc., reported 2016-01-20, distributed in AL, CA, FL, GA, ID, ME, MO, NC…. Product on the package label did not match what was inside the package. The label was for part number 00-2359-

Recall numberZ-0646-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer Biomet, Inc., Warsaw, IN, United States
Recall initiated2015-12-09
Classified2016-01-13
Reported by FDA2016-01-20
Terminated2016-11-08
DistributedAL, CA, FL, GA, ID, ME, MO, NC, NY, PA, SC, WI
Countries outside the USAE, AU, BE, BR, CA, CN, DO, FR, IN, IT, JP, MY, NL, PL, TW, UY
Quantity400
Reason classeslabeling
Lot numbers62896038, 62918019
Model numbers00-2359-014-24, 00-2359-058-35

Product

Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length; Zimmer Periarticular Locking Plate System 2.4mm Locking Screw 14 mm Length. Indicated for temporary internal fixation and stabilization of osteotomies and fractures.

Reason for recall

Product on the package label did not match what was inside the package. The label was for part number 00-2359-058-35 (Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58mm Length) lot number 62918019 while the product inside the package was part number 00-2359-014-24 (Zimmer Periarticular Locking Plate System 2.4mm Locking Screw 14mm Length) lot number 62896038.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0646-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.