Medical Depot Recalls EZ Adjust Aluminum Crutches Due to Tip Failure
Medical Depot Inc. is recalling 123,125 pairs of EZ adjust aluminum crutches because the tip may fail, posing a risk of injury.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a structural defect in a medical device that poses a risk of harm (injury) to users, but the source text does not report any specific injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.
Plain-English summary
Medical Depot Inc. is recalling 123,125 pairs of EZ adjust aluminum crutches. The recall covers adult, youth, and tall adult models sold in single-pair and eight-pair cases. The affected products are identified by item numbers 10430-1, 10430-8, 10431-1, 10431-8, 10432-1, and 10432-8.
The recall was initiated because the tip of the crutch, specifically the bottom of the metal portion that comes into contact with the ground, may fail. This defect could cause the crutch to slip or break, potentially resulting in injury to the user.
The products were distributed nationwide. Consumers who have these crutches should stop using them immediately and contact Medical Depot Inc. for instructions on how to return the product for a refund or replacement.
The recalled product
- Product
- EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, adult, 8 pairs per case, 3) EZ adjust aluminum crutch, youth, 1 pair per case, 4) EZ adjust aluminum crutch, youth, 8 pairs per case, 5) EZ…
- Manufacturer
- Medical Depot Inc.
- Category
- Medical Device — Mobility Aids
- Affected units
- 123,125
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- Item #: 1) 10430-1
- 2) 10430-8
- 3) 10431-1
- 4) 10431-8
- 5) 10432-1 & 6) 10432-8
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 6 recalled by Medical Depot Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 6 products in this recall →Related recalls
Same manufacturer · Medical Depot Inc.
See all →- SevereiGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk
FDA (Devices) · 2025-05-21
- HighKnee walker recalled for tiller separation that may cause falls
FDA (Devices) · 2024-07-24
- HighKnee Walker Tiller Separation Risk Recalled Due to Fall Hazard
FDA (Devices) · 2024-07-24
- HighMedical Depot Aluminum Crutches Recalled Due to Tip Failure
FDA (Devices) · 2016-07-06
- HighMedical Depot Universal Aluminum Crutches Recalled for Tip Failure
FDA (Devices) · 2016-07-06
Same hazard · structural failure
See all →- High
- ModerateQuantum Ops Recalls ADAPTABLE Beach Chair Surgical Patient Positioners
FDA (Devices) · 2026-10-14
- SevereMedline Bariatric Rollator Recalled Due to Front Wheel Assembly Disconnect Risk
FDA (Devices) · 2026-10-14
- SevereMedline Bariatric Rollator Recalled Due to Front Wheel Detachment Risk
FDA (Devices) · 2026-10-14
- SeverePacearth Recalls Swing Seats Due to Serious Injury Risk from Falling
CPSC · 2026-10-08
Similar recalls
- HighCook Inc. Recalls Angled Tip Ureteral Catheter Sets Due to Loading Defect
FDA (Devices) · 2020-02-12
- HighConMed Recalls Infinity ACL Tibial Tip Guides Due to Misalignment
FDA (Devices) · 2020-12-30
- HighBiomet Recalls Unilateral External Fixation Ankle Clamps Due to Assembly Error
FDA (Devices) · 2015-06-17
- HighSkytron EZ Slide Operating Table Recalled for Potential Slide Cap Detachment
FDA (Devices) · 2016-06-08
- SevereDePuy RECLAIM Hip Implant Inserter Adaptor Recalled for Fracture Risk
FDA (Devices) · 2015-04-08
- SevereAcorn 180 Curved Stairlift Recalled Due to Broken Rivets
FDA (Devices) · 2016-04-27