FDA Recall Terminated

Thio Med w/Dex, Hemin, Vit K (5ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Recall: Z-1378-2019 · Initiated April 17, 2019

Recall

Recall Number
Z-1378-2019
Event Number
82677
Firm
Remel Inc
FEI Number
1924669
Product Code
JSG
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
April 17, 2019
Terminated
August 21, 2020
Address
12076 Santa Fe Trail Dr, Lenexa, KS, 66215-3519

Description

Thio Med w/Dex, Hemin, Vit K (5ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Reason

Potential for products to fail performance testing per the Instructions for Use (IFU) starting at 57 days after date of manufacturing. Expiration date is shortened from 7 months to 56 days.

Action

Thermo Fisher Scientifica/ Remel notified consignees on about 04/17/2019 via " URGENT MEDICAL DEVICE FIELD ACTION RECALL" letter. Instructions included to locate all affected in inventory, destroy any affected product identified, contact Customer Services or local distributor to arrange for replacements, notify all customers if product was further distributed, and complete and return the Field Action Response form. Customers were also instructed that the requirement for review of reported test results using product beyond the updated expiry date should be determined by the appropriate technical expert at each customer location. Questions or concerns can be directed to Technical Services Department at 800-255-6730 (US) or 913-888-0939 (International).

Distribution

Worldwide Distribution -US Nationwide distribution to AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, VA, VT, WA, WI, WV, WY, Puerto Rico. International distribution to Singapore

Quantity

1,205 units