Gentueri Inc recalls Gentueri Viral Transport Medium (VTM), Sterile, IVD
Medium showed visual turbidity and discoloration, potentially contaminating samples transported for testing.
Read the official notice →- Date
- 2022-01-26
- Country
- United States
- Brand
- Gentueri
- Product
- Gentueri Viral Transport Medium (VTM), Sterile, IVD
- Classification
- Class II
- Units
- US Nationwide distribution in the state of Indiana.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Gentueri recalls
- 2022-02-16
US
Gentueri Inc recalls Gentueri Viral Transport Medium Kit with 8cm Breakpoint Swab
Kits failed sterility testing and showed evidence of contamination.
Other drugs & medical recalls in the United States
- 2022-01-26
US
Microbiologics Inc recalls KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC…
Contamination with S. epidermidis
FDA · DeviceMicrobiologics IncDistribution was made to CA, IA, IL, LA, MA, MI, NY, PA, SD, TN, VA, WI, and…Official notice →US
Compass Health Brands (Corporate Office) recalls Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx (RLEU10BL, RLEU10PK, RLEU10WT) RLEU10BL Voyager…
Wheel spoke may crack causing the wheel to separate from the axle may result in patient injuries, including bruising and lacerations requiring stitches.
US
Philips North America Llc recalls Infa-Therm Transport Mattress, Reference Number 989805616831 1015
After the device was cleared by the FDA, Philips made changes to the labeling that do not fall within the existing FDA clearance. These devices with the modified labeling cannot be distributed or sold without new…
US
Ortho-Clinical Diagnostics, Inc. recalls VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
Lower than expected results for VITROS¿ Immunodiagnostic Products TSH Reagent Pack when diluted with VITROS¿ Immunodiagnostic Products High Sample Diluent A Reagent Pack Lot 2190.
FDA · DeviceOrtho-Clinical Diagnostics, Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice →US
Greiner Bio-One North America, Inc. recalls greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs.,…
Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
FDA · DeviceGreiner Bio-One North America, Inc.Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA. There was…Official notice →US
Draeger Medical, Inc. recalls Draeger Fabius MRI Anesthesia Machine, Catalog Number 8607300
26 Fabius MRI Anesthesia machines were distributed with internal hoses routing Oxygen to the Oxygen Flush and Oxygen Flow Control interchanged. If the hospital O2 Central supply pressure is not stable, the O2 fresh gas…
FDA · DeviceDraeger Medical, Inc.US Nationwide distribution in the states of NY, PA, and WI.Official notice →