PlainRecalls

2023 Recalls

6,617 recalls · Page 64 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 38 critical, 10 moderate, and 2 lower-severity recalls. The page references 12 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

Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532 Spare, Optics Bench V2, L2G/LP6G

Ellex Medical Pty Ltd.

FDA Devices Critical Jul 5, 2023

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030

TELEFLEX LLC

FDA Devices Low Jul 5, 2023

Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes. Ca…

Randox Laboratories Ltd.

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080060

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380050

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Design Options¿ / Epidural anesthesia kit (10 count carton)

B. Braun Medical, Inc.

FDA Devices Moderate Jul 5, 2023

PushTracker E2 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 111780085

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380030

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170140

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150025

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during electrosurgery

Megadyne Medical Products, Inc.

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…

Remel, Inc

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181045

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080100

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170090

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780075

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in…

DRE Medical Group Inc

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082060

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during electrosurgery

Megadyne Medical Products, Inc.

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781060

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480035

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

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

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781080

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed

Baxter Healthcare Corporation

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080050

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060

TELEFLEX LLC

FDA Devices Low Jul 5, 2023

Immunoassay Premium Control Tri Level-In vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of ana…

Randox Laboratories Ltd.

FDA Devices Critical Jul 5, 2023

Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170130

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Voalte Patient Safety, Part Number 4.0, V4.0.000 to 4.0.401, used with the Centrella Bed

Baxter Healthcare Corporation

FDA Devices Critical Jul 5, 2023

Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504560

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506545

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506550

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082065

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Exactech Ergo Impactor Handle, Catalog #321-09-05.

Exactech, Inc.

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781075

TELEFLEX LLC

FDA Devices Moderate Jul 5, 2023

Vanta with AdaptiveStim Implantable Neurostimulator, Model 977006; spinal chord stimulation

Medtronic Neuromodulation

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181060

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380060

TELEFLEX LLC

FDA Devices Critical Jul 5, 2023

Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080080

TELEFLEX LLC

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.