PlainRecalls
FDA Devices Moderate Class II Ongoing

Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.

Reported: July 24, 2019 Initiated: January 17, 2019 #Z-1985-2019

Product Description

Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.

Reason for Recall

The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.

Details

Recalling Firm
DJO, LLC
Units Affected
9 units
Distribution
Distributed domestically, Oklahoma
Location
Vista, CA

Frequently Asked Questions

What product was recalled?
Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.. Recalled by DJO, LLC. Units affected: 9 units.
Why was this product recalled?
The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 24, 2019. Severity: Moderate. Recall number: Z-1985-2019.