PlainRecalls
FDA Devices Moderate Class II Terminated

StoneBreaker Sterilization Cap, Catalog number: SBA-SC; GPN: G52602; UDI: (01)00827002526020

Reported: May 9, 2018 Initiated: January 31, 2018 #Z-1594-2018

Product Description

StoneBreaker Sterilization Cap, Catalog number: SBA-SC; GPN: G52602; UDI: (01)00827002526020

Reason for Recall

The interior of the product may not be sterilized to the appropriate Sterility Assurance Level when following the reprocessing instructions in the Instructions for Use.

Details

Recalling Firm
Cook Inc.
Units Affected
470
Distribution
US Nationwide, OUS countries: AE, AT, AU, BE, BG, BR, CA, CH, CL, CN, CO, CR, CZ, DE, DJ, DK, DO, EC, EE, EG, ES, FI, FJ, FR, GB, GR, GT, HK, HN, HR, HU, ID, IE, IL, IN, IT, JO, KZ, LB, LT, LV, MA, MO, MX, MY, NI, NL, NO, NZ, PE, PH, PK, PL, PR, PT, QA, RO, RU, SA, SE, SG, SI, SK, SV, TH, TT, TW, UA, UY, XK, ZA
Location
Bloomington, IN

Frequently Asked Questions

What product was recalled?
StoneBreaker Sterilization Cap, Catalog number: SBA-SC; GPN: G52602; UDI: (01)00827002526020. Recalled by Cook Inc.. Units affected: 470.
Why was this product recalled?
The interior of the product may not be sterilized to the appropriate Sterility Assurance Level when following the reprocessing instructions in the Instructions for Use.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 9, 2018. Severity: Moderate. Recall number: Z-1594-2018.