Remel Recalls
86 recalls on record · February 13, 2013 to July 8, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 8, 2026Medical DevicesFDA
Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Hazard: Reduced or no recovery of some strains of Neisseria gonorrhoeae.
April 22, 2026Medical DevicesFDA
Remel, Inc recalls Yeastone Broth, 11ML, 10/BOX YY3462
Hazard: Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.
March 4, 2026Medical DevicesFDA
Remel, Inc recalls Campy CVA Medium 100/PK, R01272
Hazard: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
December 3, 2025Medical DevicesFDA
Remel, Inc recalls 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Hazard: Products may contain contamination, which may result in a darker or brown media color.
August 6, 2025Medical DevicesFDA
Remel, Inc recalls Blood/MacConkey Biplate 100/PK, Product Number R02049
Hazard: The products may contain surface and subsurface contamination of Listeria monocytogenes.
August 6, 2025Medical DevicesFDA
Remel, Inc recalls Blood/EMB, Levine 100/PK, Product Number R02041
Hazard: The products may contain surface and subsurface contamination of Listeria monocytogenes.
August 6, 2025Medical DevicesFDA
Remel, Inc recalls Strep Selective II Agar, Product Number R01859
Hazard: The products may contain surface and subsurface contamination of Listeria monocytogenes.
August 6, 2025Medical DevicesFDA
Remel, Inc recalls Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Hazard: The products may contain surface and subsurface contamination of Listeria monocytogenes.
June 18, 2025Medical DevicesFDA
Remel, Inc recalls Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; inv
Hazard: Product may have an off color affecting perfomance
March 26, 2025Medical DevicesFDA
Remel, Inc recalls Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Se
Hazard: Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.
February 26, 2025Medical DevicesFDA
Remel, Inc recalls remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
Hazard: Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
February 26, 2025Medical DevicesFDA
Remel, Inc recalls remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use
Hazard: Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
November 6, 2024Medical DevicesFDA
Remel, Inc recalls remel BactiDrop Acridine Orange, REF 21502, 50 per package.
Hazard: A color change of the solution within the dropper can occur from orange-yellow to light yellow resulting in out-of-specification fluorescent stain results.
September 20, 2023Medical DevicesFDA
Remel, Inc recalls remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containi
Hazard: On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target organism during customer QC testing or use with patient samples
July 5, 2023Medical DevicesFDA
Remel, Inc recalls Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk,
Hazard: The test medium may not perform as intended.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre MDRGN3F, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
December 14, 2022Medical DevicesFDA
Remel Inc recalls Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST
Hazard: An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
March 16, 2022Medical DevicesFDA
Remel Inc recalls Thermo Scientific Sensititre Gram Negative Susceptibility Testing Plate, IVD format
Hazard: There are lower than expected MICs for some gram negative species.
August 4, 2021Medical DevicesFDA
Remel Inc recalls ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
Hazard: Out of Specification
May 19, 2021Medical DevicesFDA
Remel Inc recalls Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative pr
Hazard: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.
April 21, 2021Medical DevicesFDA
Remel Inc recalls Remel Haemophilus Test Medium(100mm) 10/PK, REF: R01503 Remel Haemophilus Test Medium (HTM) is a solid medium recomm
Hazard: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may exhibit lighter than normal growth making zones difficult to measure.
April 21, 2021Medical DevicesFDA
Remel Inc recalls Remel Haemophilus Test Medium (150 mm) 10/PK, REF 04033 Remel Haemophilus Test Medium (HTM) is a solid medium recomme
Hazard: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may exhibit lighter than normal growth making zones difficult to measure.
January 20, 2021Medical DevicesFDA
Remel Inc recalls Remel Blood Agar/MacConkey Agar Bi-Plate, REF: R02049
Hazard: The blood agar side of the bi-plate may not grow some patient isolates or QC organisms as intended.