PlainRecalls

Remel Inc

Compiled from official public sources by the editorial team.

85 recalls on record · Latest: Apr 22, 2026

Remel Inc Recall Insight

Remel Inc appears on 85 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.084% 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 Apr 22, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 9 critical, 41 moderate, and 0 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 May 3, 2017 to Apr 22, 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 Apr 22, 2026

Yeastone Broth, 11ML, 10/BOX YY3462

FDA Devices Moderate Mar 4, 2026

Campy CVA Medium 100/PK, R01272

FDA Devices Moderate Dec 3, 2025

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

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 Aug 6, 2025

Blood/EMB, Levine 100/PK, Product Number R02041

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 Feb 26, 2025

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

FDA Devices Moderate Nov 6, 2024

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

FDA Devices Moderate Sep 20, 2023

remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containing mixed bacterial flora

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 Critical Dec 14, 2022

Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST

FDA Devices Critical Dec 14, 2022

Thermo SCIENTIFIC Sensititre Plate, GN4F, 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 May 19, 2021

Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative procedures as a screening metho…

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 Apr 21, 2021

Remel Haemophilus Test Medium (150 mm) 10/PK, REF 04033 Remel Haemophilus Test Medium (HTM) is a solid medium recommended for use in qualitative p…

FDA Devices Moderate Jan 20, 2021

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

FDA Devices Moderate May 20, 2020

SWIN 2017 database, Model YSW4000

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 May 29, 2019

Thio Med w/Dex, Hem, Vit K (7ml) 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/o Ind, w/Dex (18ml) 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, Hem, Vit K (9ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivatio…

FDA Devices Moderate May 29, 2019

Thio Med w/o Ind, w/Dex (9ml) 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, Hem, Vit K (10ml) 20/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/Dex, Hem, Vit K (9ml) 100/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivati…

FDA Devices Moderate Sep 19, 2018

remel THIOGLYCOLLATE MEDIUM, REF 05152

FDA Devices Moderate Sep 19, 2018

remel THIOGLYCOLLATE MEDIUM W/O INDICATOR. W/ DEXTROSE (a) 9ML, REF 064700 (b) 10ML, REF 07176 (c) 9ML, REF 064702

FDA Devices Moderate Sep 19, 2018

remel THIOGLYCOLLATE MEDIUM W/O IND. W/ DEXTROSE W/ HEMIN & VIT.K (a) 10ML, REF 07182 (b) 10ML, REF 07180 (c) 5ML, REF 064732 (d) 5ML, REF 064730…

FDA Devices Moderate Jan 3, 2018

Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum, Ref R30164201 ZH01. Product Usage: Suitable for the use in slide agglutination tests to …

FDA Devices Moderate Dec 13, 2017

CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.

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…

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Data Sources

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.