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Recall Observatory FDA recall evidence

Device product

S-Rom¿ Total Hip System Poly Liner Packaging: The insert is placed into an inner foil pouch and vacuum sealed; a ring is placed into a Tyvek/PET pouch and sealed; the foil pouch and Tyvek/PET pouch are placed into a nylon outer pouch and sealed. This is then placed into a folding carton, labeled, and shrink-wrapped. Description: Total Hip System Poly Dial¿ Liner is part of the S-ROM¿ Total Hip System. The Liner is fitted inside the acetabular shell; and is the bearing surface for the Head on the S-ROM¿ stem. The S-ROM liner is used for total hip arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. Intended Use: Total Hip System Poly Dial Liner is part of the S-Rom Total Hip System. The Liner is fitted inside the acetabular shell; and is the bearing surface for the Head on the S-Rom¿ stem. The S Rom liner is used for total hip arthroplasty is intended to provide increased patient mobility and reduce pain by replacing the damaged hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components.

Z-2414-2012

August 22, 2012

Class II

Product summary

Firm
DePuy Orthopaedics, Inc.
Event
Event 62765
Status
Terminated
Classification
Class II
Quantity
12 liners
Official record key
device-enforcement:Z-2414-2012

Official wording

Reason: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the S-ROM" liner because the Carton label has an Incorrect Color Code Series Designation. We have received one complaint regarding this issue.

Code information: Catalogue Lot Number 87-5987 3189424 3312166 3340992 3402685

Distribution pattern: Nationwide Distribution including the states of MA, TX, OH, CA, and NC.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    label has an Incorrect