PlainRecalls
FDA Devices Moderate Class II Ongoing

Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874)

Reported: October 5, 2022 Initiated: August 16, 2022 #Z-1824-2022

Product Description

Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874)

Reason for Recall

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Details

Recalling Firm
Cook Incorporated
Units Affected
204 OUS
Distribution
Domestic distribution nationwide. Foreign distribution worldwide.
Location
Bloomington, IN

Frequently Asked Questions

What product was recalled?
Amplatz extra Stiff Wire Guide, Stiff Guidewire (OUS ONLY); Reference Part Number: THSF-35-145-AES-SGH (GPN G06801) THSF-38-80-AES-SGH (GPN G06874). Recalled by Cook Incorporated. Units affected: 204 OUS.
Why was this product recalled?
Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 5, 2022. Severity: Moderate. Recall number: Z-1824-2022.