FDA Recall Terminated

Disposable Light Handle Cover, Item Number B1-715-65. Packaged 1 device inside a peel pouch and sealed. Sealed pouches are packaged 10 each inside a poly liner. 5 rows of 10 pouches are placed in a labeled corrugated mailer box. Product Usage: Intended to be used as a disposable barrier for a surgical lighting system and which allows a surgical team member to manually adjust the lighting system. Single use device.

Recall: Z-0523-2018 · Initiated October 13, 2017

Recall

Recall Number
Z-0523-2018
Event Number
78419
Firm
Ecolab, Inc.
FEI Number
3014342658
Product Code
FTA
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
October 13, 2017
Terminated
July 22, 2020
Address
940 Lone Oak Rd, Saint Paul, MN, 55121-2214

Description

Disposable Light Handle Cover, Item Number B1-715-65. Packaged 1 device inside a peel pouch and sealed. Sealed pouches are packaged 10 each inside a poly liner. 5 rows of 10 pouches are placed in a labeled corrugated mailer box. Product Usage: Intended to be used as a disposable barrier for a surgical lighting system and which allows a surgical team member to manually adjust the lighting system. Single use device.

Reason

Sterile packaging of the disposable light handle cover may contain gaps in the seal of the pouch.

Action

Ecolab sent and Urgent Medical Device Recall letter dated October 13, 2017 to customers. The identified the affected product, problem and actions to be taken. Instructions include to immediately quarantine lots in inventory, notify customers since the product has been further distributed, return affected product, and complete and return the Recall Response Form. For questions call 903-597-2568.

Distribution

Distributed domestically to Michigan.

Quantity

5,958 cases (50 per case)