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Recall company profile

Stryker Howmedica Osteonics Corp. Recalls

Overview of recall records associated with Stryker Howmedica Osteonics Corp., including dates, categories and classifications where available.

10recall records

May 31, 2017latest record date

Aug 17, 2016earliest record date

Recall history in this database

Classification mix: Class II: 10.

Medical DeviceMay 31, 2017

Stryker Howmedica Osteonics Hoffmann LRF Safety Clip (Bone Transport Strut), 14 x 12 x 5 mm recall — FDA Z-2160-2017

Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety Clip - Bone Transport Strut because there is a potential for loosening of the safety clips from the intended…

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceJan 18, 2017

Stryker Howmedica Osteonics Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg recall — FDA Z-1020-2017

Reunion TSA Peg Alignment Sound broke during surgery.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceDec 28, 2016

Stryker Howmedica Osteonics GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 recall — FDA Z-0880-2017

A review of packaging revealed the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed at one end due to a…

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceNov 16, 2016

Stryker Howmedica Osteonics LFIT Anatomic V40 Femoral Head, Low Friction Ion Treatment recall — FDA Z-0378-2017

Stryker received several complaints describing incidence of harm secondary to taper lock failure for specific lots of numerous catalog numbers of LFIT Anatomic CoCr V40 Femoral Heads.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceOct 19, 2016

Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor, REF 2101-0200 recall — FDA Z-0060-2017

Stryker Orthopaedics has received reports of the thread length protruding past the dome of the acetabular trial or implant for the Trident Universal Impactor/Positioner.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceSep 21, 2016

Stryker Howmedica Osteonics Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar Nail System recall — FDA Z-2791-2016

Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceSep 21, 2016

Stryker Howmedica Osteonics Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System recall — FDA Z-2792-2016

Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceSep 21, 2016

Stryker Orthopaedics Patella Assembly Instrument, REF 3182-1000, Non-Sterile, NDC (01) recall — FDA Z-2789-2016

Upon failure of the press-fit, the clamping sub components and pins could disassociate from the Scorpio Patella Assembly Instrument.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceAug 17, 2016

Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with Secondary Lock recall — FDA Z-2390-2016

It was reported that the secondary locking mechanism, and its corresponding components, disassociated from the Specialty Triathlon Tibial Alignment Handle with Secondary Lock Assembly…

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Medical DeviceAug 17, 2016

Stryker Howmedica Osteonics Orthopedic manual surgical instrument Usage: Exeter Rasp Handle recall — FDA Z-2396-2016

Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

Class IIFDA: TerminatedStryker Howmedica Osteonics Corp.

Understanding this recall history

This page summarizes recall records in which the official source identifies Stryker Howmedica Osteonics Corp. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.