FDA recall record

Zimmer Biomet Connecting Bolt, Model 14-442093 recall — FDA Z-2875-2018

Product was manufactured from the incorrect material, which shows a potential decrease in the fatigue strength of the connecting bolt that can lead to…

Class IIclassification
Z-2875-2018official record ID
Aug 29, 2018report date

Recall record at a glance

Official recordZ-2875-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmZimmer Biomet, Inc.
Report dateAug 29, 2018
Recall initiation dateJun 18, 2018
Quantity247 units
LocationWarsaw, IN, United States

Official product description

Connecting Bolt, Model 14-442093

Why the product was recalled

Product was manufactured from the incorrect material, which shows a potential decrease in the fatigue strength of the connecting bolt that can lead to fracture.

Distribution information

AR, AZ, CA, FL, GA, IN, KY, LA, MA, MI, MN, MO, MT, NJ, NY, OH, SC, TX, UT & WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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