Reported Sep 23, 2026 · Ongoing · Updated Sep 29, 2026

ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNEE P/S 82-3-0318 SCORPIO +…

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: Howmedica Osteonics Corp. · 325 Corporate Dr · Mahwah, NJ · 07430-2006

Is this the product you have?

  • ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNEE P/S 82-3-0318 SCORPIO + MOBILE BEARING PCS 78-5-0910 SCORPIO C-DOME PATELLA 73-2710 SCORPIO INSET PATELLA 73-2610 SCORPIO M-DOME PATELLA 73-0110 73-0710 73-0910 SCORPIO RECESSED PATELLA 26MM 3044-0026 SCORPIO TS TIB INS 72-4-9114 SCORPIO TS TIBIAL INSERT 72-4-0324 SCORPIOFLEX TOTAL KNEE CR 72-16-0512 72-16-0518 72-16-0912 72-16-1112 SERIES II TIBIAL BEAR INSERT NO 11 15MM 3052-1115 UHR BIPOLAR 26X52mm UH1-52-26 UHR BIPOLAR 26X58mm UH1-58-26 UHR BIPOLAR 28X48mm UH1-48-28 UHR BIPOLAR 28X52mm UH1-52-28 UHR BIPOLAR 28X55mm UH1-55-28 UHR BIPOLAR 32X49MM UH1-49-32 UHR BIPOLAR 32X51MM UH1-51-32 UHR BIPOLAR 32X52MM UH1-52-32 UHR BIPOLAR 32X54MM UH1-54-32 Orthopaedic implant components manufactured from UHMWPE (polyethylene)
Lot codes and dates

19 of 19 products

Products covered by this recall
#BarcodesProduct as published
104546540400635Lot 23325151 82-2-0518 UDI-DI 04546540400635
204546540400758Lot 23640051 82-2-0912 UDI-DI 04546540400758
304546540364319Lot 26862851 82-3-0318 UDI-DI 04546540364319
40761332736600607613327033847Lot 28208551 78-5-0910 UDI-DI 07613327366006 Lots 30582401 30582601 73-2710 UDI-DI 07613327033847
50761332701408207613327050288Lot 14HDSA 73-2610 UDI-DI 07613327014082 Lots 193307A 193307E 73-0110 UDI-DI 07613327050288
60761332705029507613327050332Lot HHPW 73-0710 UDI-DI 07613327050295 Lots 8P83 DL4V 73-0910 UDI-DI 07613327050332
70761332703377907613327034875Lot 14NACD 3044-0026 UDI-DI 07613327033779 Lots 14SCVA 14SCVD 14SCVF 72-4-9114 UDI-DI 07613327034875
807613327034356Lot 8H39KP 72-4-0324 UDI-DI 07613327034356
90761315402051507613154020539Lot 23505751 72-16-0512 UDI-DI 07613154020515 Lots 17376651 19093651 23125951 27835951 72-16-0518 UDI-DI 07613154020539
1007613154020652Lot 25621551 72-16-0912 UDI-DI 07613154020652
1107613154020737Lot 17879451 72-16-1112 UDI-DI 07613154020737
1207613327034240Lot 22764851 3052-1115 UDI-DI 07613327034240
1307613327017168Lot MJ7YY6 UH1-52-26 UDI-DI 07613327017168
14076133270173590761332701701407613327017182Lot 5J8PM2 UH1-58-26 UDI-DI 07613327017359 Lots 1R8TNH 414A2L 4W1HD7 AV0J7J E226XA E50DAW M31665 WK1WP2 X90ML6 UH1-48-28 UDI-DI 07613327017014 Lots N046DW N06WWP N20WDM N75AY1 P419XW RP3D0X TD218R V15WA1 VH06PA VN3P18 VR853H WM8KJT XE2ND8 YH0N93 UH1-52-28 UDI-DI 07613327017182
1507613327017281Lot V02MME UH1-55-28 UDI-DI 07613327017281
1607613327017069Lot R30MME UH1-49-32 UDI-DI 07613327017069
1707613327017120Lot 324H9H UH1-51-32 UDI-DI 07613327017120
180761332701721207613327017267Lot 9J6N9E UH1-52-32 UDI-DI 07613327017212 Lots 5D4NMJ 9T612E UH1-54-32 UDI-DI 07613327017267
19Lot MNNAAL
Amount recalled
12,156 US

This recall covers 9 products

The agency filed one notice per product. You are reading one of them; the other 8 are below.

Where it was sold

  • Nationwide

Why it was recalled

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 3:01 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.