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.
December 17, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml vials. A growth supplement for the isolation
Hazard: Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.
December 3, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of whic
Hazard: A reagent within the test may return false negative results.
December 3, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella Pneumo Groups 2-14 Latex Test, DR0802M, containing 50 tests per box. The box contains a variety of comp
Hazard: A reagent within the test may return false negative results.
December 3, 2014Medical DevicesFDA
Remel Inc recalls Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg. A stain for use in qualitativ
Hazard: The product may appear cloudy or discolored and may not perform correctly in presumptive diagnosis of mycobacterial disease.
November 19, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella BCYE Growth Supplement SR0110A, packaged in 100 ml vials, 10/pkg. A growth supplement for the isol
Hazard: Recalled product may not provide adequate recovery of Legionella pneumophila when used as directed and may result in false negative identification of Legionella pneumophila.
July 23, 2014Medical DevicesFDA
Remel Inc recalls Thermo Scientific VersaTREK REDOX 1, Ref 7102-44, 80ml with Stir Bar (O2 aerobic), 50 bottles/box, IVD. The firm name o
Hazard: Bottles did not provide positive signals within the time frame of the quality control specification for one of two strains of Streptococcus pneumoniae.
April 30, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, on
Hazard: A reagent contained within the product may return false negative results.
April 30, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of whi
Hazard: A reagent contained within the product may return false negative results.
March 26, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Vancomycin 30 mcg, each cartridge contains 50 susceptibility discs, CT0058B. The firm name on the label is Oxoid
Hazard: Some of the discs may not be impregnated with the antibiotic.
March 5, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Legionella BCYE Growth Supplement, For 500 ml of medium, SR0110C, packaged 10 vials/box, lyophilized. The firm na
Hazard: The product may contain high levels of microbial contamination
January 29, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs, Ertapenem 10 mcg., CT1761B, packaged in cartridges of 50 discs, 5 cartrid
Hazard: Cartridges may contain individual discs which were not impregnated with antibiotic.
January 29, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B, packaged in cartridges of 50 discs, 5 cartri
Hazard: Cartridges may contain individual discs which were not impregnated with antibiotic.
January 29, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs, Norfloxacin 10 mcg., CT0434B, packaged in cartridges of 50 discs, 5 cartr
Hazard: Cartridges may contain individual discs which were not impregnated with antibiotic.
January 29, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B, packaged in cartridges of 50 discs, 5 cartr
Hazard: Cartridges may contain individual discs which were not impregnated with antibiotic.
January 22, 2014Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5 ca
Hazard: Individual discs in the lot may not be sufficiently impregnated with antibiotic, resulting in smaller than expected zone sizes.
December 25, 2013Medical DevicesFDA
Remel Inc recalls Streptex* Latex D, Ref R30950901 ZL54, IVD, Latex reagent for streptococcal group D, 50 tests per box. The firm name on
Hazard: The product may give weak or false negative test results.
December 25, 2013Medical DevicesFDA
Remel Inc recalls Streptex* kit, Ref R30950501 ZL50, Rapid latex test for Streptococcal grouping, IVD. The kit contains reagent groups A,
Hazard: The product may give weak or false negative test results.
December 25, 2013Medical DevicesFDA
Remel Inc recalls remel RapID Yeast Plus System, 20 tests, Ref: R8311007, IVD, containing a 15-ml bottle of RapID Yeast Plus Reagent A and
Hazard: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and Reagent B) are mislabeled. The labels were reversed.
December 25, 2013Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg, 50 discs per cartridge, 5 cartridges per
Hazard: Boxes labeled as CIP5 may contain cartridges of AMP5.
September 4, 2013Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs,
Hazard: Use of affected lots may give false indication of susceptibility to Nitrofurantoin.
August 21, 2013Medical DevicesFDA
Remel Inc recalls Remel X/pect Flu A&B Control Swabs, For In Vitro Diagnostic Use, Ref R246003, each package contains 20 Flu A Control Sw
Hazard: Flu A+ Control Swabs incorrectly give Flu A- results when used for quality control testing with the Xpect Flu A&B test kit.
February 20, 2013Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges
Hazard: The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.
February 20, 2013Medical DevicesFDA
Remel Inc recalls Remel Xpect Clostridium difficile Toxin A/B, IVD, 40 clostridium difficile toxin A/B tests, REF 24640. Product Usage
Hazard: The firm is recalling the products due to a potential for false negative test results.
February 20, 2013Medical DevicesFDA
Remel Inc recalls Remel Xpect Clostridium difficile Toxin A/B, IVD, 20 clostridium difficile toxin A/B tests, REF 24650. Product Usa
Hazard: The firm is recalling the products due to a potential for false negative test results.
February 20, 2013Medical DevicesFDA
Remel Inc recalls The product is a lyophilized growth supplement for use with dehydrated culture media to prepare BCYE Medium used for iso
Hazard: The product may contain low level microbial contamination which could result in incorrect results.
February 13, 2013Medical DevicesFDA
Remel Inc recalls Oxoid Antimicrobial Susceptibility Test Discs, Aztreonam 30 ug, IVD, REF CT0264B, Oxoid Ltd., UK, [email protected]
Hazard: The firm is recalling the product due to some cartridges may contain individual discs that are not impregnated with antibiotic. The firm notified their customers of the recall with a notification letter and requested a confirmation fax back of receipt.