FDA Device recall Z-1933-2014
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 3. Part of the NexGen syste…
- FDA Device
- Class II
- terminated
- Published 2014-07-09
On 2014-07-09 the FDA classified a Class II recall of NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 3. Part of the NexGen syste… by Zimmer, citing zimmer is initiating a voluntary recall of specific identified lots due to the potential that the threads may be out of specification.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1933-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-19 |
| Published | 2014-07-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 3. Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.
Reason
Zimmer is initiating a voluntary recall of specific identified lots due to the potential that the threads may be out of specification.
Identifiers
| code_info | Size 3, includes the following Lot numbers: 370316 37214039 61414610 61414611 61442294 61442295 61442296 614422…Size 3, includes the following Lot numbers: 370316 37214039 61414610 61414611 61442294 61442295 61442296 61442297 61450963 61450964 61450965 61454951 61454952 61454953 61459941 61459942 61475123 61475124 61488064 61488065 61488066 61488067 61488068 61497512 61497513 61507223 61507224 61518151 61518153 61518154 61526398 61526399 61558358 61558359 61558360 61558361 61567336 61567337 61567338 61567339 61592084 61592085 61592086 61592087 61627191 61627192 61627193 61627194 61627195 61627196 61627197 61627198 61627199 61627201 61627202 61643928 61643929 61643930 61643931 61643932 61658872 61658873 61658874 61658875 61658876 61658877 61672561 61672562 61672563 61672564 61672565 61672566 61721668 61721669 61721670 61774134 61774135 61774136 61774137 61774140 61774141 61774142 61827112 61827113 61827114 61827115 61827116 61863088 61863090 61863091 61863093 61863094 61898777 61898778 61898779 6189878 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1933-2014%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.