FDA Recall Open, Classified

Stay Safe Cap

Recall: Z-0507-2024 · Initiated October 10, 2023

Recall

Recall Number
Z-0507-2024
Event Number
93396
Firm
Fresenius Medical Care Holdings, Inc.
FEI Number
3001451489
Product Code
KDJ
Status
Open, Classified
Root Cause
Labeling design
Initiated
October 10, 2023
Posted
December 7, 2023
Address
920 Winter St, Bld 920, Waltham, MA, 02451-1521

Description

Stay Safe Cap

Reason

Updating the labeling to include additional warnings and contraindications for potential side effects.

Action

Consignees were mailed an IMPORTAND MEDICAL DEVICE INFORMATION notification dated 10/10/23 vis USPS. This notification is to bring awareness to consignees that Fresenius is updating the labeling to their Stay Safe Cap to include additional warnings and contraindications for potential side effects for P/N 05-95012. Increased exposure to povidone-iodine, which is present in the Stay Safe Cap, could lead to iodine-induced hypothyroidism and hypersensitivity. Clinicians are asked to not use these devices in known cases of povidone-iodine allergy. Fresenius is updating labeling to include these medical warnings and contraindications. Any clinical or medical questions can be directed to the firm at 1-855-616-2309. Consignees are asked to return the provided Reply Form by fax to 781-966-9796 or 781-472-7413, ATTN: Quality Department, or by email to [email protected].

Distribution

US Nationwide distribution.

Quantity

18,236,160 eaches