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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 75873

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 15, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Smith & Nephew, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 3

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.

Z-0944-2017
Recall number
Z-0944-2017
Initiated
November 15, 2016
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
6266 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
All lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

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 13 71354314 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 14 71354315 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 15 71354316 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 16 71354317 REDAPT PROXIMALLY FLUTED {} STEM 240MM SZ 17 71354318 REDAPT PROXIMALLY FLUTED STEM-240MM SZ 18 71354319 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 19 71354320 REDAPTPROXIMALLY FLUTED STEM- 240MM SZ 20 71354321 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 21 71354322 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 22 71354323 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 23 71354324 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 24 71354325 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 25 71354326 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 26 71354327 REDAPT PROXIMALLY FLUTED STEM- 240MM SZ 27 71354328 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 12 71354329 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 13 71354330 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 14 71354331 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 15 71354332 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 16 71354333 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 17 71354334 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 18 71354335 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 19 71354336 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 20 71354337 REDAPT PROXIMALLY FLUTED STEM- 300MM SZ 21 71354338 REDAPT PF STEM-300MM SZ 22 71354339 REDAPT PF STEM-300MM SZ 23 71354340 REDAPT PF STEM-300MM SZ 24 71354341 REDAPT PF STEM 300MM SZ 25 71354360 REDAPT MODULAR SLVD STEM 240MM SZ 15 71354361 REDAPT MODULAR SLVD STEM 240MM SZ 16 71354362 REDAPT MODULAR SLVD STEM 240MM SZ 17 71354363 REDAPT MODULAR SLVD STEM 240MM SZ 18 71354364 REDAPT MODULAR SLVD STEM 240MM SZ 19 71354365 REDAPT MODULAR SLVD STEM 240MM SZ 20 71354366 REDAPT MOD SLVD STEM 240MM SZ 21 71354367 REDAPT MOD SLVD STEM 240MM SZ 22 71354368 REDAPT MOD SLVD STEM 240MM SZ 23 71354369 REDAPT MOD SLVD STEM 240MM SZ 24 71354370 REDAPT MOD SLVD STEM 240MM SZ 25 71354371 REDAPT MOD SLVD STEM 240MM SZ 26 71354372 REDAPT MOD SLVD STEM 240MM SZ 27 71354374 REDAPT MOD SLVD STEM 300MM SZ 12 71354375 REDAPT MOD SLVD STEM 300MM SZ 13 71354376 REDAPT MOD SLVD STEM 300MM SZ 14 71354377 REDAPT MOD SLVD STEM 300MM SZ 15 71354378 REDAPT MOD SLVD STEM 300MM SZ 16 71354379 REDAPT MOD SLVD STEM 300MM SZ 17 71354380 REDAPT MOD SLVD STEM 300MM SZ 18 71354381 REDAPT MOD SLVD STEM 300MM SZ 19 71354382 REDAPT MOD SLVD STEM 300MM SZ 20 71354383 REDAPT MOD SLVD STEM 300MM SZ 21 71354384 REDAPT MOD SLVD STEM 300MM SZ 22 71354385 REDAPT MOD SLVD STEM 300MM SZ 23 71354386 REDAPT MOD SLVD STEM 300MM SZ 24 71354387 REDAPT MOD SLVD STEM 300MM SZ 25 71354388 REDAPT MOD SLVD STEM 300MM SZ 26 71354389 REDAPT MOD SLVD STEM 300MM SZ 27 71354404 REDAPT PF STEM 300MM SZ 26 71354405 REDAPT PF STEM 300MM SZ 27 71354407 REDAPT MOD SLEEVED STEM 240MM SZ 12 71354408 REDAPT MOD SLVD STEM 240MM SZ 13 71354409 REDAPT MODULAR SLVD STEM 240MM SZ 14 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 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

Distribution pattern

Worldwide Distribution - US (nationwide) and Internationally to Austria, Australia, Belgium, Canada, Switzerland, China, Cyprus, Czech Republic, Dubai, Germany, Denmark, Spain, France, United Kingdom, Greece, Hong Kong, India, Italy, Mexico, Netherlands, Poland, Puerto Rico, Portugal, Russia, Turkey, and South Africa.

device · product 2 of 3

Modular SMF(TM) 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.

Z-0945-2017
Recall number
Z-0945-2017
Initiated
November 15, 2016
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
11999 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
All lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

71352401 SMF STEM RSA SIZE 1 71352402 SMF STEM RSA SIZE 2 71352403 SMF STEM RSA SIZE 3 71352404 SMF STEM RSA SIZE 4 71352405 SMF STEM RSA SIZE 5 71352406 SMF STEM RSA SIZE 6 71352407 SMF STEM RSA SIZE 7 71352408 SMF STEM RSA SIZE 8 71352409 SMF STEM RSA SIZE 9 71352501 SMF STEM WITH STIKTITE SZ 1 71352502 SMF STEM WITH STIKTITE SZ 2 71352503 SMF STEM WITH STIKTITE SZ 3 71352504 SMF STEM WITH STIKTITE SZ 4 71352505 SMF STEM WITH STIKTITE SZ 5 71352506 SMF STEM WITH STIKTITE SZ 6 71352507 SMF STEM WITH STIKTITE SZ 7 71352508 SMF STEM WITH STIKTITE SZ 8 71352509 SMF STEM WITH STIKTITE SZ 9

Distribution pattern

Worldwide Distribution - US (nationwide) and Internationally to Austria, Australia, Belgium, Canada, Switzerland, China, Cyprus, Czech Republic, Dubai, Germany, Denmark, Spain, France, United Kingdom, Greece, Hong Kong, India, Italy, Mexico, Netherlands, Poland, Puerto Rico, Portugal, Russia, Turkey, and South Africa.

device · product 3 of 3

Modular Necks: 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.

Z-0946-2017
Recall number
Z-0946-2017
Initiated
November 15, 2016
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
13671 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
All lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

71352111 STANDARD OFFSET NEUTRAL MODULAR NECK 71352112 HIGH OFFSET NEUTRAL MODULAR NECK 71352116 LEFT ANTEVERTED MODULAR NECK 71352117 RIGHT ANTEVERTED MODULAR NECK 71354061 MOD NECK HO +10 NECK HEIGHT 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.

Distribution pattern

Worldwide Distribution - US (nationwide) and Internationally to Austria, Australia, Belgium, Canada, Switzerland, China, Cyprus, Czech Republic, Dubai, Germany, Denmark, Spain, France, United Kingdom, Greece, Hong Kong, India, Italy, Mexico, Netherlands, Poland, Puerto Rico, Portugal, Russia, Turkey, and South Africa.