Data Foundry

Medical device recalls 2018

Zimmer M/L Taper Hip Prosthesis — Class II medical device recall Z-1191-2018

Terminated recall by Zimmer Biomet, Inc., reported 2018-04-04, distributed in AZ, CA, CT, IN, MD, MI, MN, NJ…. Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip implant, actually contained a Siz

Recall numberZ-1191-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer Biomet, Inc., Warsaw, IN, United States
Recall initiated2018-03-01
Classified2018-03-26
Reported by FDA2018-04-04
Terminated2019-07-18
DistributedAZ, CA, CT, IN, MD, MI, MN, NJ, NY, OR, PR, WA
Countries outside the USCN, IN
Quantity12
Reason classeslabeling
UPC / GTIN / UDI-DI00889024131736
Lot numbers63716611
Model numbers00-7711-007-40

Product

Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size 7.5 Extended Offset Reduced Neck Length; Part Number: 00-7711-007-40

Reason for recall

Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip implant, actually contained a Size 4 Standard Reduced Neck length taper hip implant.

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-1191-2018. 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.