Reported Aug 27, 2014 · Terminated

PS Tibial Insert, REF 163-1XXX Product Usage: UHMWPE component used in TKA procedures to serve as a tibial bearing…

Ortho Development Corporation

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: Ortho Development Corporation · 12187 Business Park Dr · Draper, UT · 84020-8663

Is this the product you have?

  • PS Tibial Insert
  • REF 163-1XXX Product UsageUHMWPE component used in TKA procedures to serve as a tibial bearing surface for articulation with the femoral component
Lot codes and dates

6 of 6 products

Products covered by this recall
Model / numberProduct as published
163-1309Lot A135943,PS Tibial Insert Size 3 9mm
163-1312Lot A136492,PS Tibial Insert Size 3 12mm
163-1407Lot A136453,PS Tibial Insert Size 4 7mm
163-1407Lot A135945,PS Tibial Insert Size 4 7mm
163-1509Lot A136454,PS Tibial Insert Size 5 9mm
Lot A135827
Amount recalled
11

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide
  • VA

Why it was recalled

Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial Insert, UC Tibila Insert, and CK Tibil Insert because the foil pouches did not properly seal, allowing air to seep back into the pouch after sealing which increases the risk that the material properties of the implant would be substantially degraded due to oxidation.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Oct 6, 2014 · Data as of Sep 19, 6:01 PM UTC

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