Reported Oct 19, 2016 · Terminated
Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor, REF 2101-0200, Non-Sterile, Howmedica Osteonics…
Stryker Howmedica Osteonics Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Howmedica Osteonics Corp. · 325 Corporate Dr · Mahwah, NJ · 07430-2006
Is this the product you have?
- Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor, REF 2101-0200, Non-Sterile, Howmedica Osteonics Corp., Mahwah, NJ, USA, A Subsidiary of Stryker Corp.
- Lot codes and dates
- Catalog No
362 of 362 codes
2101-0200Lot Nos. SMM7A00SMM7A00LSMM7A02SMM7A02ASMM7A02ESMM7A02EESMM7A01TSMM7A01TTSMM7A01TDSMM7A01TDDSMM7C02HSMM7C02SMM7C01SMM7C01TSMM7C01TTSMM7C01WSMM7E03SMM7E03ASMM7E00SMM7A00ESMM7E02SMM7E02ASMM7E01SMM7E01ASMM7K00. SMM7K01SMM7K01ASMM7K03SMM7K03LSMM7K02SMM7K02TSMM7K03XSMM7K03YSMM7C02JSMM7L00HSMM7L00JSMM7L00KSMM7L00SMM7C01TWSMM7M01SMM7A02TSMM7M00SMM7M00ASMM7M02HSMM7M02SMM7E02MSMM7E01JKSMM7K03JSMM7K00ASMM6N04SMM7N01JSMM7N01SMM7M06SMM7M09SMM7N03SMM7N03ASMM7M06ASMM7M09SMM7N00SMM7M05
- Catalog No
- Amount recalled
- 3,768 units
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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