PlainRecalls

2023 Recalls

6,617 recalls · Page 66 of 133

2023 Recall Year Insight

Federal agencies issued 6,617 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.51% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 18.1 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 133 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 35 critical, 15 moderate, and 0 lower-severity recalls. The page references 14 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 Jul 5, 2023

Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy samples from soft tissue and tumors of the breast REF: SERTERA-14

Hologic, Inc

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Jul 5, 2023

RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.

Appliedvr

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170135

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504575

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382025

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080090

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780070

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R

Limacorporate S.p.A

FDA Devices Moderate Jul 5, 2023

Access Hybritech p2PSA reagent, REF B03704 and REF A49752.

Beckman Coulter, Inc.

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080085

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 3, Right

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504565

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

wDR 2.2 Mobile Digital Diagnostic X-Ray System

SEDECAL SA

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082055

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during electrosurgery

Megadyne Medical Products, Inc.

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Right

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150035

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Verigene Enteric Pathogens Nucleic Acid Test (EP), REF 30-002-023

Luminex Corporation

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506525

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180035

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Perifix¿ / Epidural anesthesia kit (10 count carton)

B. Braun Medical, Inc.

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150030

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

PushTracker E3 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D, MX2-33P, MX2-33PK…

Permobil

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780050

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382040

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080095

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180045

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS

Covidien, LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380040

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during electrosurgery

Megadyne Medical Products, Inc.

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506540

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170150

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180055

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480025

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-…

Phadia US Inc

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Exactech Shoulder GPS Impactor Handle, Catalog #531-07-05.

Exactech, Inc.

FDA Devices Moderate Jul 5, 2023

EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA GliadinDP IgG is intended for the in vitro semi-quantitative…

Phadia US 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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2023 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.