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Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indi...

FDA Device Recall #Z-0944-2017 — Class II — November 15, 2016

Recall Summary

Recall Number Z-0944-2017
Classification Class II — Moderate risk
Date Initiated November 15, 2016
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Smith & Nephew, Inc.
Location Memphis, TN
Product Type Devices
Quantity 6266 units

Product Description

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 for Recall

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

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.

Lot / 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

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Frequently Asked Questions

Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

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