FDA recall Z-1906-2023

Ossur H / F · Class II · device

Product

Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200; Icelock 621 Ratchet, REF: L-621000; Icelock 621 Ratchet Adaption Kit, REF: L-621100; Ratchet Lock Body, REF: L-692020

Reason for recall

A mechanical lock used to connect and release a locking liner into a prosthetic socket have an attachment pin and lock that can wear down faster than expected, leading to the potential for the pin to disengage from the lock, leading to loss of suspension of the external prosthetic system that replaces a missing lower limb, which can lead to falling and injury.

Distribution

US: SC, FL,NM, PA, VA, CA, TX, MT, UT, OH, NV, KS, MI, GA, IA, WA, TN, AZ, MN, NC, IN, MS, AL, NY, ID, DE, OK, MA, WI, OR, KY, MD, CO, WV, LA, IL, NJ, CT, MO, NE, WY, AR, SD, PR

Key facts

Status
Ongoing
Initiation date
2023-05-12
Report date
2023-06-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Reykjavik, N/A, Iceland

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1906-2023