PlainRecalls

2023 Recalls

6,535 recalls · Page 130 of 131

2023 Recall Year Insight

Federal agencies issued 6,535 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 7.78% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.9 recalls per day across the FDA, CPSC, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 131 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2023.

On this page of 50 records, severity classification shows 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 8 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ — an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2023 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number — always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PREVI COLOR GRAM REAGENT NOZZLE CLEANING SOLUTION (NA), CATALOG 29588

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part Number: 376630

Beaver Visitec International, Inc.

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS, CATALOG 423102

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

API NIT1 NIT2 REAGENTS, CATALOG 70442

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

BIOBALL A.BRASILIENSIS NCPF 2275 550X20, CATALOG 56011

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CHROMID STREPTO B US 20 PLT, CATALOG 419751

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

BIOBALL K.RHIZOPHILA (30X20), CATALOG 412690

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN70 TEST KIT 20 CARDS, CATALOG 413401

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VERIFY Dual Species Self-Contained Biological Indicators, 100 per box Item Number: S3061 Intended for use in installation testing and routine mon…

Steris Corporation

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

Liquid Assayed Specific Protein- In vitro diagnostic use, in the quality control of serum on clinical chemistry and immunoassay systems Catalog Numb…

Randox Laboratories Ltd.

FDA Devices Moderate Jan 11, 2023

Detect Covid-19 Test Product/Model Number: 21205

Detect Headquarters

FDA Devices Moderate Jan 11, 2023

Guardian iOS app (MMT-8200) and Guardian Android app (MMT-8201), part of the Guardian 4 system

Medtronic MiniMed

FDA Devices Moderate Jan 11, 2023

PPM CLINICAL CRAPONNE CHROMID C.DIFFICILE 20 PLT, CATALOG 43871

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

DeRoyal Tonsillectomy Tray, REF 89-10698.01

DeRoyal Industries Inc

FDA Devices Moderate Jan 11, 2023

BECKMAN COULTER IRISpec CA/CB/CC control, REF 900-7211, For in vitro diagnostic use only.

Beckman Coulter, Inc.

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS ESTRADIOL II 60 TESTS, CATALOG 30431-01

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PPM INDUSTRY COMBOURG BACARA 20PLATES 90MM, CATALOG AEB520100

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

API VP1 VP2 REAGENTS, CATALOG 70422

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS T PHOSPHATE BUFFERSTERILE 20X9ML, CATALOG T8035

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

API JAMES 2AMP, CATALOG 70542

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412240

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN69 TEST KIT 20 CARDS, CATALOG 413400

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VIDAS CLINICAL VIDAS LH 60 TESTS, CATALOG 30406-01

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL BENZYLPENICIL PG 256 US S30, CATALOG 412262

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS CT&IR&DB-TSA + L & P80 10PLT, CATALOG C6045-IR

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PPM LOMBARD PRODUCTS IR&DB - TSA (32ML) 10PLT, CATALOG M1205-IR

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

BIOBALL P.AERUGINOSA NCTC 12924 550X20, CATALOG 56017

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL FLUCONAZOLE FL 256 US S30, CATALOG 412333

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use, in the quality control of serum on clinical chemistry and immunoassay syste…

Randox Laboratories Ltd.

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

PREVI COLOR GRAM REAGENT IODINE-B (NA), CATALOG 29586

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT AST-GN95 TEST KIT 20 CARDS, CATALOG 421982

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS, CATALOG 21343

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

VITEK 2 REAGENT GP TEST KIT VTK2 20 CARDS, CATALOG 21342

Biomerieux Inc

FDA Devices Moderate Jan 11, 2023

ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, CATALOG 412252

Biomerieux Inc

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2023 with 2022 →

Data Sources

  • Source: FDA openFDA Enforcement API — calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA — consumer product and vehicle recall feeds for 2023