VERSA-FX II STD TUBE 130DX16H, 130DX18H, 130DX20H, 135DX16H, 135DX18H, 135DX20H, 140DX16H, 140DX18H, 140DX20H, 145DX16H, 145DX18H, 145DX20H, 150DX16H, 150DX18H, 150DX20H
Check against the official notice below — it lists the full affected range.
Zimmer Biomet is recalling 510 VERSA-FX II STD TUBE implants in various sizes due to packaging design verification test failures. The implants are sterile-packaged in single package configurations and were distributed domestically across all U.S. states and Puerto Rico, as well as internationally to numerous countries including Canada, Australia, Japan, China, and others. The affected products are identified by specific lot numbers and item numbers listed in the recall record.
The recall affects implants with lot numbers ranging from 60528430 through 63197443 and item numbers from 00119313016 through 00119315020. The source document does not specify a remedy or action for affected consumers to take.
Written by software from the official notice below. Not reviewed by a lawyer.
Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.
Reason for recall: Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures. Distribution: Domestic: Puerto Rico, AK AL AR AZ CA CO CT FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WY Foreign: CANADA, ALGERIA ARGENTINA AUSTRALIA BELGIUM BRAZIL BRIDGEND WALES CHINA DUBAI UAE EGYPT EL SALVADOR ENGLAND ESCHBACH GERMANY EXPORT DORAL FL FRANCE GERMANY GUATEMALA HONDURAS INDIA ITALY JAMAICA JAPAN JORDAN KOREA LEBANON Quantity: 510 Lot/code info: 510K:K150818,K954555 Item Numbers: 00119313016 00119313018 00119313020 00119313516 00119313518 00119313520 00119314016 00119314018 00119314020 00119314516 00119314518 00119314520 00119315016 00119315018 00119315020 Lot Numbers: 60528430 60528430R 367587 368766 368965 369002 368935 61067765 61067765R 61020321 61020321R 369009 61086830 61140159 61151192 61163286 61163286R 61151212 61246966 61244915 61314528 61314528R 61309346 61326723 61326723R 369454 61309347 61309347R 369477 369477R 61352928 61352928R 369558 369837 369823 61625238 61776782 37107690 45003072 37213895 37214379 62388915 62311351 62511283 62547278 62430175 62547305 62461668 62388917 62445943 62430159 62547286 37109076 37109075 37109077 62931598 62950756 62993953 62934787 63004526 63028872 62970952 62993347 62779484 63010741 62986294 62993353 63197443
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.