The Recall Desk
ModerateFDA (Devices)·Z-2086-2020·Announced 2020-05-27

Stryker Restoration Anatomic Shell Recalled Due to Packaging Defect

Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Shells because the device may fall off its post in the inner packaging, resulting in loose coating debris.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, but the source text describes a packaging defect without reporting any illnesses, injuries, or hospitalizations, fitting the criteria for a moderate severity precautionary recall.

Plain-English summary

Howmedica Osteonics Corp. is recalling Stryker Restoration Anatomic Hemispherical Shells, Size 56 Left, Sterile. The recall involves 4,895 units distributed worldwide, including numerous U.S. states.

The recall is being conducted because the Stryker Restoration Anatomic Shell may fall off its post within its inner packaging. This defect can result in the device being loose in the package with coating debris.

Healthcare providers and facilities that have received these specific devices should stop using them and contact Howmedica Osteonics Corp. for further instructions on how to return or dispose of the affected units.

The recalled product

Product
Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 56 Left, Sterile, Catalog # 504-02-56D-L, UDI (01)07613327012361(17)
Affected units
4,895

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • Lot #s 4J3N24
  • W03J5W
  • N119A4
  • WK7K99
  • NM70TR
  • 3376L4
  • RK3XRL
  • RH27YA
  • M00KML
  • TM2MMK
  • PW30H8
  • DL01A0
  • WD4T0V
  • 2D40YA
  • 4Y5LAE
  • W63A8E
  • VJ34EV
  • AR5H0T
  • HY6Y45
  • KV2835

Distribution

Part of a larger recall action

This product is one of 16 recalled by Howmedica Osteonics Corp. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 16 products in this recall →