Thio Med w/Dex, Hem, Vit K(10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Class I - Dangerous
🏥 Medical Devices Recalled: April 17, 2019 Remel Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Material Number: R07180; Lot Number (Labeled Expiration Date): 314206 (12/20/2018), 315673 (12/25/2018), 322659 (01/07/2019), 330648 (01/21/2019), 333828 (01/24/2019), 337102 (01/31/2019), 343936 (02/14/2019), 347392 (02/28/2019), 353577 (03/06/2019), 366056 (03/28/2019), 367423 (04/02/2019), 370220 (04/09/2019), 377044 (04/22/2019), 380480 (04/29/2019), 390571 (05/16/2019), 391563 (05/20/2019), 407306 (06/20/2019), 418374 (07/18/2019).
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Remel Inc
Reason for Recall:
Potential for products to fail performance testing per the Instructions for Use (IFU) starting at 106 days after date of manufacturing. Expiration date is shortened from 9 months to 105 days.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Thio Med w/Dex, Hem, Vit K(10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Product Codes/Lot Numbers:

Material Number: R07180; Lot Number (Labeled Expiration Date): 314206 (12/20/2018), 315673 (12/25/2018), 322659 (01/07/2019), 330648 (01/21/2019), 333828 (01/24/2019), 337102 (01/31/2019), 343936 (02/14/2019), 347392 (02/28/2019), 353577 (03/06/2019), 366056 (03/28/2019), 367423 (04/02/2019), 370220 (04/09/2019), 377044 (04/22/2019), 380480 (04/29/2019), 390571 (05/16/2019), 391563 (05/20/2019), 407306 (06/20/2019), 418374 (07/18/2019).

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1407-2019

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