RecallRadar

FDA Device recall Z-1027-2018

VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 CALCAR 15.5X180MM STR +20 CALCAR 16.5X180MM STR Prosthesis, Hip, Semi-Constrained, Me…

On 2018-03-21 the FDA classified a Class II recall of VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 CALCAR 15.5X180MM STR +20 CALCAR 16.5X180MM STR Prosthesis, Hip, Semi-Constrained, Me… by Zimmer Biomet, citing the LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant af….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1027-2018
ClassificationClass II
Statusterminated
Initiated2017-11-29
Published2018-03-21
Last updated2026-09-13 11:54 UTC
CompanyZimmer Biomet
DistributionUS

Product

VERSYS 7.5 IN BEADED FC +10 CALCAR 13.5X180MM STR +10 CALCAR 15.5X180MM STR +20 CALCAR 16.5X180MM STR Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Reason

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Identifiers

code_info
Item Number: 00-7843-013-07 Lot Numbers: 61946025 61735805 61993658 61768679 62029060 61815080 62043103 618794…Item Number: 00-7843-013-07 Lot Numbers: 61946025 61735805 61993658 61768679 62029060 61815080 62043103 61879441 77000599 Item Number: 00-7843-015-07 Lot Number: 62135320 Item Number: 00-7843-016-17 Lot Numbers: 61879439 61993648

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1027-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.