Recall Z-2105-2016— Medical Depot Inc.
Class II · Terminated
Class II FDA medical device recall by Medical Depot Inc., initiated 2016-02-17, terminated 2018-06-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.. Reason: Tip crutch failure involving the bottom of the metal portion which comes in contact with ground.
- Recalling firm
- Medical Depot Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-02-17
- Terminated
- 2018-06-13
- Firm location
- Port Washington, NY, United States
Product description
Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
Reason for recall
Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Data sourced from openFDA. This site is unofficial and independent of the FDA.