PlainRecalls

Remel, Inc

Compiled from official public sources by the publisher.

86 recalls on record · Latest: Jul 8, 2026

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Agency notice ledger

Federal filing book Remel, Inc MID-BOOK · SINGLE-AGENCY

#207 of 14,151 · 86 notices · 0.082% archive

  • BOOK 86 notices
  • RANK #207 of 14,151
  • SHARE 0.082% archive
  • AGENCY FDA Devices (86)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jul 8, 2026
  • PHOTO Beacon Hill Medical P…

Nearest notice-volume peer: Beacon Hill Medical Pharmacy, P.C. (0 notice gap)

Remel, Inc accounts for about 0.082% of the 104,423-notice archive on 86 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Remel, Inc's standing among 14,151 recalling firms

Remel, Inc ranks 207th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Remel, Inc vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

86 207th of 14151 higher than 13,943 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Remel, Inc in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Remel, Inc holds about 0.082% of archive notices alongside 86 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Jul 8, 2026

GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
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 YV4000-VZ
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 Diagnostic Use.
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 method for primary isolation and presumptive identification of vancomycin-resistance enterococci (VRE) from surveillance cultures.
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 procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests with Haemophilus species.
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 procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests with Haemophilus species.
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 cultivation of aerobes and anaerobes
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 of aerobes and anaerobes
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 of aerobes and anaerobes
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 of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 cultivation of aerobes and anaerobes
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 (e) 9ML, REF 064720
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 identify Shigella cultures presumptively for epidemiological and diagnostic purposes.
FDA Devices Moderate Dec 13, 2017

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

Remel, Inc carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Carestream Health, Inc. 86 ROi Cps LLC 86 Stryker Howmedica Osteonics Corp. 87 Cook Incorporated 85

Frequently Asked Questions

How many federal recall notices name Remel, Inc? ▼
PlainRecalls indexes 86 distinct federal recall events naming Remel, Inc, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Remel, Inc sit among other recalling firms? ▼
Remel, Inc ranks #207 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Remel, Inc's notices? ▼
FDA Devices accounts for 86 of this firm's 86 indexed notices.
What product category dominates Remel, Inc's filing book? ▼
Filings for Remel, Inc span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Remel, Inc: 86 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Remel, Inc; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026