FDA Recall Terminated

SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult

Recall: Z-1366-2021 · Initiated February 8, 2021

Recall

Recall Number
Z-1366-2021
Event Number
87432
Firm
Sharp Medical Products
FEI Number
3017828726
Product Code
GCJ
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
February 8, 2021
Terminated
February 17, 2023
Address
14362 N Frank Lloyd Wright Blvd, Scottsdale, AZ, 85260-8846

Description

SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult

Reason

Non-conformity (holes/punctures or deep creases) in the sterile barrier.

Action

On 02/08/2021 the firm began notifying customers and received confirmation that affected lot was still on customers shelves. On 03/03/2021, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Notification Letter via certified US mail informing customers that they have become aware of product that either have holes or deep creases in the sterile barrier that makes the product unsafe for use and could lead to patient infection, sepsis, or death if used. Customer are instructed: 1.That any/all remaining units on their shelves should be disposed of in the trash. 2. Complete "MEDICAL DEVICE RECALL RETURN RESPONSE Acknowledgement and Receipt Form and scan and send via email to [email protected] or send via mail to attention of Carolyn Urish at 14362 N Frank Lloyd Wright, Scottdales AZ, 85260. Any questions or further guidance - contact the Recalling Firm at email [email protected] or by phone at 630-232-8002 ext. 5 Monday through Friday 8:00 a.m. to 4:30 p.m. Mountain Time.

Distribution

U.S.: AZ, FL, MI, OH, TX, and WI. O.U.S.: None

Quantity

129 units (63 units for Human-use and 66 units for Non-Human use)