The Recall Desk
ModerateFDA (Devices)·Z-1487-2019·Announced 2019-05-29

Zimmer GmbH Recalls CBS Micro Countersink Cannulated AO Screws

Zimmer GmbH is recalling CBS micro, countersink, cannulated, AO screws (Item Number ST503004541) because they may have been manufactured from a different material than specified.

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 does not report any hospitalizations, injuries, or illnesses. The hazard is a potential material deviation without confirmed adverse health consequences, fitting the criteria for a moderate severity score.

Plain-English summary

Zimmer GmbH is recalling CBS micro, countersink, cannulated, AO screws, Item Number ST503004541. The recall was initiated after an investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.

The affected products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY. All items marked with "Normed" are affected.

Healthcare providers and facilities should stop using the affected products and contact Zimmer GmbH for further instructions. Consumers should not use these medical devices and should consult their healthcare provider if they have questions regarding their use.

The recalled product

Product
CBS micro, countersink, cannulated, AO, Item Number ST503004541
Manufacturer
Zimmer GmbH

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 (1)

  • All items marked with "Normed" are affected

Distribution

Part of a larger recall action

This product is one of 76 recalled by Zimmer GmbH 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 76 products in this recall →