Data Foundry

Medical device recalls 2024

JuggerLoc/ToggleLoc 2 — Class II medical device recall Z-0477-2025

Ongoing recall by Biomet, Inc., reported 2024-11-27, distributed nationwide. Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result

Recall numberZ-0477-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBiomet, Inc., Warsaw, IN, United States
Recall initiated2024-10-21
Classified2024-11-15
Reported by FDA2024-11-27
DistributedNationwide (US)
Countries outside the USAU, BR, CA, CH, SG
UPC / GTIN / UDI-DI00880304857254
Lot numbers0002446326, 0002446333, 0002452241, 0002453378, 0002467342, 0002476076, 0002476077, 0002476078, 0002481506, 0002481724, 0002486540, 0002486541, 0002490256, 0002493107, 0002496066, 0002497715, 0002497716, 0002500871, 0002500872, 0002504026, 0002504027, 0002504031, 0002504032, 0002504033, 0002504034, 0002504035, 0002504036, 0002504037, 0002504546, 0002513868, 0002517982, 0002517983, 0002527929, 0002527931, 0002528042, 0002528043, 0002528044, 0002528045, 0002544040, 0002592614 and 11 more
Model numbers110027357

Product

JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357

Reason for recall

Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to surgical intervention.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0477-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.