2023 Recalls
5,513 recalls · Page 55 of 111
2023 Recall Year Insight
Federal agencies issued 5,513 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.57% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 15.1 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 111 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 34 critical, 15 moderate, and 1 lower-severity recalls. The page references 20 distinct recalling firms operating in 8 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (29), FDA Food (12), CPSC (4), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555
TELEFLEX LLC
MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780045
TELEFLEX LLC
LEGACY SMARTBASE, NE 3.0D 1MML, REF: 8730-81NE; LEGACY SMARTBASE, NE 3.0D 2MML, REF 8730-82NE; LEGACY SMARTBASE NARROW NE 3.5D, REF: 8735-80NNE; L…
Implant Direct Sybron Manufacturing LLC
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504580
TELEFLEX LLC
Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170125
TELEFLEX LLC
Slick Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 150040
TELEFLEX LLC
MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
Megadyne Medical Products, Inc.
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
TELEFLEX LLC
DigitalDiagnost C90, Model No. 712034 and 712035
Philips North America Llc
Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504590
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
TELEFLEX LLC
Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781050
TELEFLEX LLC
MERCEDES-BENZ 2022-2023: ELECTRICAL SYSTEM:WIRING
MERCEDES-BENZ
MERCEDES-BENZ 2023: ELECTRICAL SYSTEM:WIRING
MERCEDES-BENZ
Bose Recalls Acoustimass®, Lifestyle® and Companion™ Bass Modules Due to Fire Hazard
Bose Corporation, of Framingham, Mass.
CaTeam Recalls Canvas Baby Hammock Swings Due to Suffocation Hazard; Violation of Safe Sleep for Babies Act on Inclined Infant Sleep Products
CaTeam, of Oak Harbor, Washington
H-E-B Recalls Leather Woven Chairs Due to Fall Hazard (Recall Alert)
UD Surya Abadi Furniture, of Indonesia
Victrola Recalls Bluetooth Record Players Due to Fire Hazard
ACURA,HONDA 2020-2023: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER
ACURA,HONDA
Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ingredients: Fish Protein (Pollock, Threadfin Bream and/or Flying Fish), Water, Potato Starc…
Aquamar Inc
Julian's Recipe Maple & Brown Butter Cauli-Wafels, 7.41 oz.
Julian's Recipe, LLC
Wegmans Penne Rigate Mozzarella Salad Net Wt 30 OZ (1 LB 14 OZ) 850 g. Packaged in a plastic container.
ASK Foods Inc
Kanimi Crab Flavored Seafood Fancy Shred Style 92410 Ingredients: Fish Protein (Pollock, Whiting and or Threadfin Bream), Water, Potato Starch, Modif…
Aquamar Inc
Wegmans Italian Classics Diavolo Pasta Sauce 24 OZ
LiDestri Foods, Inc.
Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin Bream), Water, Potato Starch…
Aquamar Inc
Julian's Recipe Original Cauli-Wafels, 7.41 oz.
Julian's Recipe, LLC
Julian's Recipe CAULI-WAFEL SANDWICHES TURKEY SAUSAGE & CHEDDAR,
Julian's Recipe, LLC
TYR Anamix Early Years infant formula Net Wt. 14.1 oz (400g) UPC: 749735002186 Product is a powder packed metal cans. 6 cans per case.
Nutricia North America
EARTH KRATOM TRAINWRECK 150 CAPSULES (UPC: 908193737324) (50 UNITS/CASE) and 300 CAPSULES (UPC: 005821990011) (25 UNITS/CASE). DISTRIBUTED BY FIRE WH…
Fire Distributors Plus LLC
EARTH KRATOM RED MAENG DA KRATOM 65 CAPSULES (UPC: 212223242796) (100 UNITS/CASE). DISTRIBUTED BY FIRE WHOLESALE. Ingredients: Mitragyna speciosa lea…
Fire Distributors Plus LLC
enterade Advanced Oncology Formula; Original Vanilla Flavor; Medical Food; Helps manage and maintain GI function; 8 FL OZ (237 mL); Recommended Use: …
ENTRINSIC HEALTH SOLUTION INC
ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited Bachupally-500 090 India, …
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01
Aurolife Pharma, LLC
ICD-DR DDBB2D1 EVERA XT IS1/DF1 INTL, Model Number DDBB2D1; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
ICD-DR DDMC3D1 EVERA MRI S OUS/US DF1, Model Number DDMC3D1; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
ICD DDPA2D1G COBALT XT DR MRI DF1 GOLD, Model Number DDPA2D1G; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRT-D DTBB2D4 VIVA S IS1/DF4 INTL, Model Number DTBB2D4; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRT-D DTBA2QQ VIVA QUAD XT IS4/DF4 INTL, Model Number DTBA2QQ; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRT-D DTBA1Q1 VIVA QUAD XT IS4/DF1 US, Model Number DTBA1Q1; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Masimo LNCS TC-I SpO2, Reusable Ear Sensor, REF: 2503
Masimo Corporation
CRTD CROME HF MRI IS1 DF4, Model Number DTPC2D4; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRTD DTMA2D1 CLARIA MRI OUS DF1, Model Number DTMA2D1; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRTD DTMC1D1 COMPIA MRI US DF1, Model Number DTMC1D1; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRTD DTMB1D4 AMPLIA MRI US DF4, Model Number DTMB1D4; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
ICD-VR VISIA AF S US/OUS IS1/DF1, Model Number DVAC3D1; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
CRT-D DTBC2QQ BRAVA QUAD IS4/DF4 INTL, Model Number DTBC2QQ; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
ICD COBALT XT HF QUAD OUS, Model Number DTPA2QQG; Implantable Cardioverter Defibrillators
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
Data Sources
- Source: FDA openFDA Enforcement API — calendar-year recall filings for food, drugs, and devices
- Source: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2023
Read our methodology — how this data is sourced, computed, and verified.