RecallRadar

FDA Device recall Z-2102-2016

EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, a…

On 2016-07-06 the FDA classified a Class II recall of EZ adjust aluminum crutch under the following labels: 1) EZ adjust aluminum crutch, adult, 1 pair per case, 2) EZ adjust aluminum crutch, a… by Medical Depot, citing tip crutch failure involving the bottom of the metal portion which comes in contact with ground.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2102-2016
ClassificationClass II
Statusterminated
Initiated2016-02-17
Published2016-07-06
Last updated2026-09-13 11:54 UTC
CompanyMedical Depot
DistributionUS

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 adjust aluminum crutch, tall adult, 1 pair per case & 6) EZ adjust aluminum crutch, tall adult, 8 pairs per case

Reason

Tip crutch failure involving the bottom of the metal portion which comes in contact with ground

Identifiers

code_infoItem #: 1) 10430-1, 2) 10430-8, 3) 10431-1, 4) 10431-8, 5) 10432-1 & 6) 10432-8

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2102-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.