PlainRecalls

Remel Inc

56 recalls on record · Latest: Mar 4, 2026

Remel Inc Recall Insight

Remel Inc appears on 56 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.067% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Mar 4, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 7 critical, 41 moderate, and 2 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 4, 2013 to Mar 4, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Mar 4, 2026

Campy CVA Medium 100/PK, R01272

FDA Devices Moderate Aug 6, 2025

Blood Agar,5% Sheep Blood 100/PK, Product Number R01202

FDA Devices Moderate Aug 6, 2025

Blood/MacConkey Biplate 100/PK, Product Number R02049

FDA Devices Moderate Aug 6, 2025

Strep Selective II Agar, Product Number R01859

FDA Devices Moderate Jun 18, 2025

Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic device

FDA Devices Moderate Mar 26, 2025

Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV40…

FDA Devices Moderate Feb 26, 2025

remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

FDA Devices Moderate Nov 6, 2024

remel BactiDrop Acridine Orange, REF 21502, 50 per package.

FDA Devices Moderate Jul 5, 2023

Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Dia…

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre MDRGN3F, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST

FDA Devices Moderate Mar 16, 2022

Thermo Scientific Sensititre Gram Negative Susceptibility Testing Plate, IVD format

FDA Devices Moderate Aug 4, 2021

ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom

FDA Devices Moderate Apr 21, 2021

Remel Haemophilus Test Medium(100mm) 10/PK, REF: R01503 Remel Haemophilus Test Medium (HTM) is a solid medium recommended for use in qualitative …

FDA Devices Moderate Jan 20, 2021

Remel Blood Agar/MacConkey Agar Bi-Plate, REF: R02049

FDA Devices Moderate May 29, 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 cultiva…

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (18ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation …

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation …

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation…

FDA Devices Moderate May 29, 2019

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 cultivat…

FDA Devices Moderate May 29, 2019

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 cultiv…

FDA Devices Moderate May 29, 2019

Thio Med w/Dex, Hem, Vit K(10ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivati…

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation o…

FDA Devices Moderate Sep 19, 2018

remel THIOGLYCOLLATE MEDIUM, REF 05152

FDA Devices Moderate May 3, 2017

Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recomm…

FDA Devices Moderate Mar 15, 2017

Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,

FDA Devices Moderate Jun 15, 2016

Oxoid Nitrocefin (+ Reconstitution Fluid Batch) REF: SR0112C, Oxoid Ltd. For the rapid chromogenic detection of beta-lactamase activity in bacterial…

FDA Devices Moderate Dec 23, 2015

Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10), REF# CT0024B packaged in packs of 5 cartridges - 50 disc/cartridge. Used in …

FDA Devices Moderate Aug 19, 2015

PathoDx Strep Grouping Kit, REF 62025, packaged 60 tests per kit. Latex agglutination test for identification of beta-hemolytic streptococci of …

FDA Devices Moderate Aug 19, 2015

PathoDx Strep B Grouping Latex, REF 62031, 3 ml packaged in plastic dropper bottle with a pink cap. Latex reagent for streptococcal group B; Ide…

FDA Devices Moderate Jul 1, 2015

VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and recovering microorganisms, espec…

FDA Devices Moderate Mar 11, 2015

Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basings…

FDA Devices Moderate Dec 3, 2014

Remel TB Potassium Permanganate (.5% Aqueous) 40192, packaged in 250 ml bottles, 5/pkg. A stain for use in qualitative procedures as a counterstai…

FDA Devices Moderate Dec 3, 2014

Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Lat…

FDA Devices Moderate Nov 19, 2014

Oxoid Legionella BCYE Growth Supplement SR0110A, packaged in 100 ml vials, 10/pkg. A growth supplement for the isolation of Legionella.

FDA Devices Moderate Apr 30, 2014

Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Gr…

FDA Devices Moderate Apr 30, 2014

Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumo…

FDA Devices Moderate Mar 26, 2014

Oxoid Vancomycin 30 mcg, each cartridge contains 50 susceptibility discs, CT0058B. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire,…

FDA Devices Moderate Jan 29, 2014

Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on t…

FDA Devices Moderate Jan 29, 2014

Oxoid Antimicrobial Susceptibility Test Discs, Norfloxacin 10 mcg., CT0434B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on …

FDA Devices Moderate Jan 22, 2014

Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5 cartridges per pack, 50 discs p…

FDA Devices Moderate Dec 25, 2013

Streptex* Latex D, Ref R30950901 ZL54, IVD, Latex reagent for streptococcal group D, 50 tests per box. The firm name on the label is Remel Inc., Len…

FDA Devices Low Dec 25, 2013

Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg, 50 discs per cartridge, 5 cartridges per box. The firm name on the b…

FDA Devices Moderate Dec 25, 2013

remel RapID Yeast Plus System, 20 tests, Ref: R8311007, IVD, containing a 15-ml bottle of RapID Yeast Plus Reagent A and a 10-ml bottle of RapID Yeas…

FDA Devices Low Sep 4, 2013

Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm …

Nearby Manufacturers

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds