Lower riskMedical device recall · FDA · Published October 21, 2024
Biomet JuggerLoc/ToggleLoc 2.9mm Drill Guide Recall: Warped Guides May Cause Surgery
Biomet recalls 2.9mm Drill Guides (Model 110027357) due to warping in packaging that may delay surgery or cause tissue reactions. Affected units include specific lots sold in the US.
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.
Take action
Contact the company
📍Recalling firmBiomet, Inc.56 E Bell Dr · Warsaw, IN 46582-6989
“Biomet JuggerLoc/ToggleLoc 2.9mm Drill Guide Recall: Warped Guides May Cause Surgery.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53675-biomet-juggerloc-toggleloc-2-9mm-drill-guide-recall-warped-guides. Based on FDA recall #Z-0477-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0477-2025%22&limit=1).
The FDA announced on 2024-10-21 that Biomet, Inc. is recalling JuggerLoc/ToggleLoc 2.9mm Drill Guides due to warping risks. The agency stated the issue may lead to extended surgery or adverse tissue reactions requiring intervention.
The FDA reported that guides were found to be warped when pulled from packaging. This defect may result in the extension of surgery to find another product or lead to adverse local tissue reactions requiring surgical intervention.
Context
GovInfoNow's records show Biomet, Inc. has had 28 other recalls on record since 2018-02-28. Other recent recalls of similar products include Biomet Intramedullary Bone Saw Blade Recall (2026-07-01), Biomet ZipT (2025-09-23), and Biomet Juggerknot Mini Soft Anchors Recall (2025-09-09). Other recent recalls of similar products include Zimmer Off-Axis Alliance Glenoid Reamer Guide Recall (2026-05-20), Zimmer Off-Axis Shoulder System Guide Recall (2026-05-20), and Zimmer Off-Axis Alliance Glenoid Reamer Guide Recall (2026-05-20).
How to tell if you have this one
Check for the model number 110027357 on the product. Affected units include specific lots listed in the recall notice (e.g., 0002446326 through 0002614123).
Brand
Biomet
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for the lot numbers listed in the recall notice (e.g., 0002446326 through 0002614123) on the product packaging.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Australia, Brazil, Canada, Singapore, Switzerland.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-0477-2025 (October 21, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0477-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.