medical MODERATE Updated 2026-09-23

Howmedica Osteonics Corp. recalls SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-00

See all recalls from Howmedica Osteonics Corp. →

Recalled Product

SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032 Orthopaedic implant components manufactured from UHMWPE (polyethylene)

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 3045-0026 No UDI Lots 12WAHA 12WAHB HOHE HOVX 3045-0028 No UDI Lots 13VAW 13VAWA 3045-0030 No UDI Lots BIYIE HNZY 3045-0032 No UDI Lots BIYIH HOYK

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for SCORPIO RECESSED METAL BACKED →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Medline Industries, LP recalls Convenience kits CATARACT PACK DYNJ59881A

2026-09-23 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

Bard Access Systems, Inc. recalls DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150

2026-09-23 · this is a downstream recall of class I recall RES 98777

Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), dilator set L, Model Numbe

2026-09-23 · The packaging may not consistently maintain sterile barrier integrity.

Medical Action Industries, Inc. 306 recalls Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451;

2026-09-23 · Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection.