FDA Device recall Z-0944-2017

Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and…

FDA Device
Class II
terminated
Published 2017-01-11

On 2017-01-11 the FDA classified a Class II recall of Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and… by Smith And Nephew, citing all lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0944-2017
Classification	Class II
Status	terminated
Initiated	2016-11-15
Published	2017-01-11
Last updated	2026-09-13 11:54 UTC
Company	Smith And Nephew
Distribution	US

Product

Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also indicated for inflammatory degenerative joint disease including rheumatoid arthritis, arthritis secondary to a variety of diseases and anomalies, and congenital dysplasia; treatments of nonunion, femoral neck fracture and trochanteric fractures of the proximal femur with head involvement that are unmanageable using other techniques; endoprosthesis, femoral osteotomy, or Girdlestone resection; fracture-dislocation of the hip; and correction of deformity. The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are intended for single use only and are to be implanted without bone cement.

Reason

All lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.

Identifiers

code_info	71354001 MDF REV IMPLANT 240MM SZ 11 71354002 MDF REV IMPLANT 240MM SZ 13 71354003 MDF REV IMPLANT 240MM SZ 14 713… 71354001 MDF REV IMPLANT 240MM SZ 11 71354002 MDF REV IMPLANT 240MM SZ 13 71354003 MDF REV IMPLANT 240MM SZ 14 71354004 MDF REV IMPLANT 240MM SZ 15 71354005 MDF REV IMPLANT 240MM SZ 16 71354006 MDF REV IMPLANT 240MM SZ 17 71354007 MDF REV IMPLANT 240MM SZ 18 71354008 MDF REV IMPLANT 240MM SZ 19 71354009 MDF REV IMPLANT 240MM SZ 20 71354011 MDF REV IMPLANT 240MM SZ 21 71354012 MDF REV IMPLANT 240MM SZ 23 71354013 MDF REV IMPLANT 240MM SZ 25 71354015 MDF REV IMPLANT 300MM SZ 11 71354016 MDF REV IMPLANT 300MM SZ 13 71354017 MDF REV IMPLANT 300MM SZ 14 71354018 MDF REV IMPLANT 300MM SZ 15 71354019 MDF REV IMPLANT 300MM SZ 16 71354021 MDF REV IMPLANT 300MM SZ 17 71354022 MDF REV IMPLANT 300MM SZ 18 71354023 MDF REV IMPLANT 300MM SZ 19 71354024 MDF REV IMPLANT 300MM SZ 20 71354025 MDF REV IMPLANT 300MM SZ 21 71354026 MDF REV IMPLANT 300MM SZ 23 71354027 MDF REV IMPLANT 300MM SZ 25 71354312 REDAPT PF STEM 240MM SZ 12 71354313 REDAPT PROXIMALLY FLUTED STEM 240MM SZ

code_info

71354001 MDF REV IMPLANT 240MM SZ 11 71354002 MDF REV IMPLANT 240MM SZ 13 71354003 MDF REV IMPLANT 240MM SZ 14 713…

71354001 MDF REV IMPLANT 240MM SZ 11 71354002 MDF REV IMPLANT 240MM SZ 13 71354003 MDF REV IMPLANT 240MM SZ 14 71354004 MDF REV IMPLANT 240MM SZ 15 71354005 MDF REV IMPLANT 240MM SZ 16 71354006 MDF REV IMPLANT 240MM SZ 17 71354007 MDF REV IMPLANT 240MM SZ 18 71354008 MDF REV IMPLANT 240MM SZ 19 71354009 MDF REV IMPLANT 240MM SZ 20 71354011 MDF REV IMPLANT 240MM SZ 21 71354012 MDF REV IMPLANT 240MM SZ 23 71354013 MDF REV IMPLANT 240MM SZ 25 71354015 MDF REV IMPLANT 300MM SZ 11 71354016 MDF REV IMPLANT 300MM SZ 13 71354017 MDF REV IMPLANT 300MM SZ 14 71354018 MDF REV IMPLANT 300MM SZ 15 71354019 MDF REV IMPLANT 300MM SZ 16 71354021 MDF REV IMPLANT 300MM SZ 17 71354022 MDF REV IMPLANT 300MM SZ 18 71354023 MDF REV IMPLANT 300MM SZ 19 71354024 MDF REV IMPLANT 300MM SZ 20 71354025 MDF REV IMPLANT 300MM SZ 21 71354026 MDF REV IMPLANT 300MM SZ 23 71354027 MDF REV IMPLANT 300MM SZ 25 71354312 REDAPT PF STEM 240MM SZ 12 71354313 REDAPT PROXIMALLY FLUTED STEM 240MM SZ

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-0944-2017%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.