PlainRecalls
FDA Devices Moderate Class II Ongoing

Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the surgical site.

Reported: August 26, 2020 Initiated: August 3, 2020 #Z-2818-2020

Product Description

Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the surgical site.

Reason for Recall

The products were improperly heat treated.

Details

Recalling Firm
Smith & Nephew, Inc.
Units Affected
111 units
Distribution
US states: CA CO CT GA HI IL IN KY MA MD NC NY OK PA SD TN WA WI OUS countries: AE CO JP KR PL ZA
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
Single RIKKI Retractor, Catalog #71934609 - Product Usage: is used during surgery to hold soft tissue away from the surgical site.. Recalled by Smith & Nephew, Inc.. Units affected: 111 units.
Why was this product recalled?
The products were improperly heat treated.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 26, 2020. Severity: Moderate. Recall number: Z-2818-2020.