FDA Device recall Z-2948-2020
PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2 PHAC1202 PROFEMUR N…
- FDA Device
- Class II
- ongoing
- Published 2020-09-16
On 2020-09-16 the FDA classified a Class II recall of PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2 PHAC1202 PROFEMUR N… by Microport Orthopedics, citing microPort Orthopedics Inc. is voluntarily recalling any existing inventory of PROFEMUR¿ Titanium and Cobalt Chrome modular necks with previous package insert versions to replace t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2948-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-07-31 |
| Published | 2020-09-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Microport Orthopedics |
| Distribution | US |
Product
PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2 PHAC1202 PROFEMUR NECK NEUTRAL SHORT COBALT CHROME PHAC1204 PROFEMUR NECK NEUTRAL LONG COBALT CHROME PHAC1212 PROFEMUR NECK A/R VAR/VAL 2 SHORT COBALT CHROME PHAC1214 PROFEMUR NECK A/R VAR/VAL 2 LONG COBALT CHROME PHAC1222 PROFEMUR NECK A/R VAR/VAL 1 SHORT COBALT CHROME PHAC1224 PROFEMUR NECK A/R VAR/VAL 1 LONG COBALT CHROME PHAC1232 PROFEMUR NECK A/R 8DG SHORT COBALT CHROME PHAC1234 PROFEMUR NECK A/R 8DG LONG COBALT CHROME PHAC1242 PROFEMUR NECK A/R 15DG SHORT COBALT CHROME PHAC1244 PROFEMUR NECK A/R 15DG LONG COBALT CHROME PHAC1252 PROFEMUR NECK VAR/VAL 8DG SHORT COBALT CHROME PHA01202 PROFEMUR NECK NEUTRALSHORT SHORT PHA01204 PROFEMUR NECK NEUTRAL LONG PHA01206 PROFEMUR NECK NEUTRAL X LONG PHA01212 PROFEMUR NECK A/R VAR/VAL 2 SHORT PHA01214 PROFEMUR NECK A/R VAR/VAL 2 LONG PHA01222 PROFEMUR NECK A/R VAR/VAL 1 SHORT PHA01224 PROFEMUR NECK A/R VAR/VAL 1 LONG PHA01232 PROFEMUR NECK 8DG A/R SHORT PHA01234 PROFEMUR NECK 8DG A/R LONG PHA01236 PROFEMUR NECK 8DG A/R X LONG PHA01242 PROFEMUR NECK 15DG A/R SHORT PHA01244 PROFEMUR NECK 15DG A/R LONG PHA01252 PROFEMUR NECK 8DG VAR/VAL SHORT PHA01254 PROFEMUR NECK 8DG VAR/VAL LONG PHA01256 PROFEMUR NECK 8DG VAR/VAL X LONG PHA01262 PROFEMUR NECK 15DG VAR/VAL SHORT PHA01264 PROFEMUR NECK 15DG VAR/VAL LONG Intended Use: MPO Total Hip Systems are indicated for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.
Reason
MicroPort Orthopedics Inc. is voluntarily recalling any existing inventory of PROFEMUR¿ Titanium and Cobalt Chrome modular necks with previous package insert versions to replace the PROFEMUR¿ Hip System Package Insert with the most recent revision (150803-8).
Identifiers
| code_info | All lots 1431860 1435705 1430154 1431065 1431308 1436522 1437003 0298131491437686 06113732261437685 128653165…All lots 1431860 1435705 1430154 1431065 1431308 1436522 1437003 0298131491437686 06113732261437685 1286531651437687 1430775 1431243 1431309 1431622 1431825 1431864 1432439 1432440 1433425 1433430 1433432 1433433 1434152 1435449 1435602 1435699 1435700 1436524 1436526 1436556 1437004 W123831741436428 1433424 1434969 14080361437684 1433431 1434993 1436525 1436527 1436528 1438068 1438130 1435702 1437055 1438069 1438131 1438455 X013918551437840 14277201440118 1434151 1434965 1435450 1435701 1435727 1435728 1436529 1436557 1436713 1438245 1438609 1438456 1438775 1438776 0398262151439704 1435603 1436712 1438872 1439145 V072510101439739 W0989675B1439738 1437581 1437877 1438664 1438873 1439144 1439379 1439380 1439387 1439582 U06811981440149 U06811981440151 V062154321440171 V092442911440169 1432436 1434964 1436365 1439944 1439945 1439946 W063349591440289 W073506871440084 1437451 1437582 1438953 14395 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2948-2020%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.