FDA recall record

Ossur H / F Icelock 125 Ratchet, REF: L-125000 recall — FDA Z-1906-2023

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…

Class IIclassification
Z-1906-2023official record ID
Jun 21, 2023report date

Recall record at a glance

Official recordZ-1906-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOssur H / F
Report dateJun 21, 2023
Recall initiation dateMay 12, 2023
Quantity4,190
LocationReykjavik, N/A, Iceland

Official product description

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

Why the product was recalled

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 information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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