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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Remel Inc: 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.

Agency Publication Date: May 20, 2019
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Affected Products

Product: Thio Med w/Dex, Hem, Vit K (5ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Lot Number (Expiration Date): 298222 (11/22/2018), 298278 (11/26/2018), 309142 (12/12/2018), 314202 (12/20/2018), 318109 (12/27/2018), 321247 (01/02/2019), 321615 (01/03/2019), 322654 (01/07/2019), 323445 (01/08/2019), 323457 (01/08/2019), 325888 (01/10/2019), 325891 (01/10/2019), 327637 (01/15/2019), 328656 (01/16/2019), 328730 (01/16/2019), 331413 (01/22/2019), 332316 (01/23/2019), 333823 (01/24/2019), 334609 (01/28/2019), 335243 (01/29/2019), 336083 (01/30/2019), 337937 (02/05/2019), 340117 (02/07/2019), 340303 (02/07/2019), 340777 (02/11/2019), 341993 (02/12/2019), 343924 (02/14/2019), 344723 (02/18/2019), 344727 (02/18/2019), 345317 (02/19/2019), 345632 (02/20/2019), 345635 (02/20/2019), 346533 (02/21/2019), 346643 (02/21/2019), 346668 (02/26/2019), 346710 (02/27/2019), 347381 (02/28/2019), 356316 (03/12/2019), 357251 (03/13/2019), 357252 (03/13/2019), 359078 (03/18/2019), 359887 (03/19/2019), 360823 (03/20/2019), 360813 (03/20/2019), 362019 (03/21/2019), 366795 (04/01/2019), 366791 (04/01/2019), 367418 (04/02/2019), 370206 (04/09/2019), 371226 (04/10/2019), 372100 (04/11/2019), 373087 (04/15/2019), 373799 (04/16/2019), 376324 (04/18/2019), 377039 (04/22/2019), 377642 (04/23/2019), 378521 (04/24/2019), 379725 (04/25/2019), 380472 (04/29/2019), 381210 (04/30/2019), 381231 (05/01/2019), 382455 (05/02/2019), 384276 (05/06/2019), 385228 (05/07/2019), 386110 (05/08/2019), 388169 (05/13/2019), 390399 (05/16/2019), 393235 (05/22/2019), 395637 (05/27/2019), 396586 (05/29/2019), 396645 (05/30/2019), 397090 (06/04/2019), 397589 (06/05/2019), 397583 (06/05/2019), 398225 (06/06/2019), 399822 (06/11/2019), 409550 (06/26/2019), 412073 (06/28/2019), 413484 (07/04/2019), 413493 (11/29/2018), 470812 (05/07/2019).

Lot Numbers:
Number
Product: 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

Lot Number (Expiration Date): 328725 (01/16/2019), 345633 (02/20/2019), 346706 (02/27/2019), 385229 (05/07/2019), 396646 (05/30/2019), 399823 (06/11/2019).

Lot Numbers:
Number
Product: Thio Med w/Dex, Hem, Vit K (7ml) 20/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Lot Number (Expiration Date): 303285 (09/27/2018), 309151 (10/10/2018), 353575 (01/02/2019).

Lot Numbers:
Number
Product: Thio Med w/Dex, Hem, Vit, K (7ml) 100/PK Product Usage; Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

Lot Number (Expiration Date): 309152 (10/10/2018), 337708 (12/03/2018), 353574 (01/02/2019), 378524 (02/20/2019).

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82677
Status: Resolved
Manufacturer: Remel Inc
Manufactured In: United States
Units Affected: 4 products (8,615 units; 1,205 units; 133 units; 242 units)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.