Data Foundry

Medical device recalls 2015

Metasul Femoral Head — Class II medical device recall Z-1136-2015

Terminated recall by Zimmer Gmbh, reported 2015-03-04, distributed in AK, AL, AR, AZ, CA, CT, DE, FL…. Potential compromise of the inner sterile tray. If a compromised tray is detected, a delay in surgery may resu

Recall numberZ-1136-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer Gmbh, Winterthur, N/A, Switzerland
Recall initiated2014-12-17
Classified2015-02-20
Reported by FDA2015-03-04
Terminated2015-09-23
DistributedAK, AL, AR, AZ, CA, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY
Countries outside the USCA, JP
Quantity16
Reason classessterility
Lot numbers61487614
Model numbers734028800

Product

Metasul Femoral Head - indicated for total hip arthroplasty for treatment of patient conditions of non-inflammatory degenerative joint disease.

Reason for recall

Potential compromise of the inner sterile tray. If a compromised tray is detected, a delay in surgery may result. If undetected breach in both the inner and outer trays were to occur, and there is contamination present, a periprosthetic infection is possible, which could lead to revision.

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-1136-2015. 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.