FDAFDA · Alimentos y medicamentos·N.º oficial Z-1377-2019
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
Publicado el 29 de mayo de 2019 · Inicio del retiro: 17 de abril de 2019
Estado reportado al momento de publicación: Terminated — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.
Qué peligro representa
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.
Qué hacer
Voluntary: Firm initiated · Letter
Detalles del retiro
- Fabricante
- Remel Inc
- Distribuidor
- 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
- Lote
- 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).
- Clasificación de riesgo
- Class II
- Área (FDA)
- device
- País
- United States
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