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Lower risk Medical device recall · FDA · Published August 3, 2018

Zimmer Biomet Drill Bit Recall: Expired Label Risk

Zimmer Biomet recalls certain long flex drill bits due to incorrect expiration date on labels. This may lead to using expired medical devices. Affected items have specific lot numbers.

🇺🇸 FDA recall #Z-3252-2018Medical deviceZimmer Biomet ›
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Recalling firmZimmer Biomet, Inc.56 E Bell Dr · Warsaw, IN 46582-6989
✎ GovInfoNow plain-language explainer

What happened, in plain English

Zimmer Biomet is recalling specific long flex drill bits used in soft tissue to bone repairs because their expiration dates are listed incorrectly on the labels. This could mean the devices are expired and unsafe for medical use. Read more at govinfonow.com/recall/70194-zimmer-biomet-drill-bit-recall-expired-label-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/70194-zimmer-biomet-drill-bit-recall-expired-label-risk · Updated August 20, 2026 · FDA enforcement record: FDA #Z-3252-2018

Cite this page

“Zimmer Biomet Drill Bit Recall: Expired Label Risk.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/70194-zimmer-biomet-drill-bit-recall-expired-label-risk. Based on FDA recall #Z-3252-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3252-2018%22&limit=1).

Why it’s dangerous

The expiration date on the label is incorrect, which means the drill bits could be expired. Using expired medical devices might lead to improper healing or infection risks during surgery.

Who’s affected

Medical professionals who purchased the recalled drill bits with lot numbers 053940, 545740, 067490, 664610, 165770, 676180, 165830, 688250, 415590, or 860050 are likely affected. Surgeons and orthopedic specialists using these bits for shoulder, foot and ankle, knee, hand and wrist, or hip repairs are at most risk.

How to tell if you have this one

Check the label for the lot numbers: 053940, 545740, 067490, 664610, 165770, 676180, 165830, 688250, 415590, or 860050. These drill bits are used for soft tissue to bone repairs in shoulder, foot and ankle, knee, hand and wrist, or hip procedures.

  • Brand
    Zimmer Biomet
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Label for Lot Number

    Look for the lot numbers listed: 053940, 545740, 067490, 664610, 165770, 676180, 165830, 688250, 415590, or 860050 on the drill bit packaging.

Where it went and when

Where it was distributed

Distributed in 10 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “AZ CO FL FL GA LA MA MA MO NY SC TX” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, Colorado, Florida, Georgia, Louisiana, Massachusetts, Missouri, New York, South Carolina, Texas.

Recall timeline

FDA terminated this recall 20 months after the firm started it.

1. Firm started the recall: Aug 3, 201812. FDA classified it Class II: Sep 26, 201823. Published in FDA’s Enforcement Report: Oct 3, 201834. FDA terminated the recall: Apr 10, 2020420182020
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-3252-2018 (August 3, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3252-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA