FDA recall Z-2390-2021

Aspen Surgical Products, Inc. · Class II · device

Product

Norton Arm Kit, Product Code 711400, (previous product code 031001), Sample Kit S711400

Reason for recall

Affected products were manufactured with materials found to have a bioburden level exceeding the limit at which the product's sterilization process was validated. As a result, the firm cannot provide full assurance that the affected products were effectively sterilized, and the product may compromise a sterile field and increase the risk of a surgical site infection.

Distribution

US nationwide distribution. No foreign distribution.

Key facts

Status
Terminated
Initiation date
2021-07-23
Report date
2021-09-08
Termination date
2022-07-26
Voluntary/Mandated
Voluntary: Firm initiated
Location
Caledonia, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2390-2021