JuggerLocJuggerLoc Slotted ReamerRecalls & reported problems across all models
Biomet Orthopedics, LLC · 3 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 3 models of JuggerLocJuggerLoc Slotted Reamer by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
JuggerLocJuggerLoc Slotted Reamer recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Feb 14, 2022Class IITerminated
Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical intervention, and/or extension of surgery to find another part.
Z-0809-2022 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗
JuggerLocJuggerLoc Slotted Reamer models
3 models, most reported first. Each model has its own page with its reports, recalls and device details.
- JuggerLoc™JuggerLoc™ Slotted Reamer 110018275Fastener, fixation, nondegradable, soft tissue1 recall0 reports
- JuggerLoc™JuggerLoc™ Slotted Reamer 110010372Fastener, fixation, nondegradable, soft tissue1 recall0 reports
- JuggerLoc™JuggerLoc™ Slotted Reamer 110010373Fastener, fixation, nondegradable, soft tissue1 recall0 reports
Other Biomet Orthopedics, LLC products
- AFFIXUSHIP FRACTURE NAIL - RIGHT39 models · 6 reports · 37 recalls
- AFFIXUSHIP FRACTURE NAIL - LEFT27 models · 7 reports · 24 recalls
- Compress Device71 models · 99 reports · 22 recalls
- Arcos Modular Revision Hip System71 models · 191 reports · 19 recalls
- Comprehensive Reverse Shoulder57 models · 895 reports · 3 recalls
- Vanguard Knee System147 models · 306 reports · 13 recalls
- STAGEONE17 models · 0 reports · 18 recalls
- StageOne Select15 models · 2 reports · 15 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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