Medical DeviceMay 5, 2021
DJ Orthopedics de Mexico S.A. de C.V DONJOY REF:11-0472-9 ULTRASLING PRO ER/IR 30 recall — FDA Z-1513-2021
failed rivet at the chafe tab of arm sling.
Class IIFDA: TerminatedDJ Orthopedics de Mexico S.A. de C.V.
Recall history in this database
Classification mix: Class II: 4.
Medical DeviceMay 5, 2021
DJ Orthopedics de Mexico S.A. de C.V DONJOY REF:11-0473-9 ULTRASLING PRO AB, UNIVERSAL, Rx recall — FDA Z-1514-2021
failed rivet at the chafe tab of arm sling.
Class IIFDA: TerminatedDJ Orthopedics de Mexico S.A. de C.V.
Medical DeviceMay 5, 2021
DJ Orthopedics de Mexico S.A. de C.V DONJOY REF:11-0447-9-ULTRASLING PRO, UNIVERSAL, Rx recall — FDA Z-1511-2021
failed rivet at the chafe tab of arm sling.
Class IIFDA: TerminatedDJ Orthopedics de Mexico S.A. de C.V.
Medical DeviceMay 5, 2021
DJ Orthopedics de Mexico S.A. de C.V DONJOY REF:11-0471-9 ULTRASLING PRO ER/IR 15 recall — FDA Z-1512-2021
failed rivet at the chafe tab of arm sling.
Class IIFDA: TerminatedDJ Orthopedics de Mexico S.A. de C.V.
Understanding this recall history
This page summarizes recall records in which the official source identifies DJ Orthopedics de Mexico S.A. de C.V. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.