Data Foundry

Medical device recalls 2016

Hgp ii acetabular cup bone screw selftap 6 — Class II medical device recall Z-1683-2016

Terminated recall by Zimmer Manufacturing B.V., reported 2016-05-25, distributed nationwide. A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

Recall numberZ-1683-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer Manufacturing B.V., Mercedita, PR, United States
Recall initiated2016-05-04
Classified2016-05-16
Reported by FDA2016-05-25
Terminated2017-07-05
DistributedNationwide (US)
Countries outside the USAR, AU, BR, CA, CL, CN, DE, ES, FR, GB, HK, IN, IT, JP, KR, SE, SG, SV, TW
Quantity1,199
Reason classessterility
Lot numbers63245682, 63276975, 63276976, 63276977, 63276979, 63276980, 63301523, 63303436

Product

Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp ii acetabular cup bone screw selftap 6.5x20mm 00662406520 Hgp ii acetabular cup bone screw selftap 6.5x25mm 00662406525 Hgp ii acetabular cup bone screw selftap 6.5x35mm 00662406535 Hgp ii acetabular cup bone screw selftap 6.5x55mm 00662406550 Hgp ii acetabular cup bone screw selftap 6.5x60mm 00662406560

Reason for recall

A small hole may be present in the inner tray of specific lots of sterile Hip and Trauma Implant Screws.

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-1683-2016. 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.