PlainRecalls

2023 Recalls

6,617 recalls · Page 40 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 5 critical, 42 moderate, and 3 lower-severity recalls. The page references 22 distinct recalling firms operating in 6 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), FDA Drug (20), FDA Food (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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Critical Aug 30, 2023

Team Fresh & Go: Pineapple Cup, packaged in 12oz plastic cup with lid. Packaged and sold as single unit.

Freshy Foods, LLC

FDA Food Critical Aug 30, 2023

Soft Zero on the Go brand Lite Peanut Butter flavor; 8 fl oz; UPC 0-91404-15285-3

Real Kosher Ice Cream, Inc.

FDA Food Critical Aug 30, 2023

Soft Serve on the Go brand Sorbet Strawberry Mango Sorbet flavor; 8 fl oz; UPC 0-91404-15128-3

Real Kosher Ice Cream, Inc.

FDA Food Moderate Aug 30, 2023

Multiple FDA-regulated products. Pallets

Inmar Supply Chain Solutions, LLC

FDA Drug Moderate Aug 30, 2023

activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured for: All USA …

Ecometics, Inc.

FDA Drug Moderate Aug 30, 2023

Helix Pain Relieving Cream (Menthol 7.4%), packaged in a) 5 gm pouch (NDC 30775-051-01), b) 3 fl. oz. roll-on (NDC 30775-051-03), c) 4 fl. oz. tubes …

Parker Laboratories, Inc.

FDA Drug Moderate Aug 30, 2023

Rufinamide Tablets, USP 400 mg, packaged in 120-count bottle, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, Ea…

Aurobindo Pharma USA Inc.

FDA Drug Moderate Aug 30, 2023

Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for Co…

Ecometics, Inc.

FDA Drug Moderate Aug 30, 2023

AstrinGyn (Ferric Subsulfate) Aqueous, 259 mg/g, 8 gm Single Use Vials, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6065-0, Ref 60…

Ecometics, Inc.

FDA Drug Moderate Aug 30, 2023

ALCOLADO RELAMPAGO (Menthol and Camphor), 1% and 1.5% respectively, packaged in a 7 FLUID OZ (207 ml) bottles, UPC 7 18864 20102 9 and b) 16 FLUID OZ…

Ecometics, Inc.

FDA Drug Moderate Aug 30, 2023

Helix Tri-Active Therapy Cream (Camphor 3.2%, Menthol 7.4%, Methyl salicylate 12.5%), packaged in a) 3 fl. oz. roll-on (NDC 30775-052-03) and b) 4 fl…

Parker Laboratories, Inc.

FDA Drug Moderate Aug 30, 2023

Blis-To-Sol Liquid (Tolnaftate), 1%, packaged in a) 1 FLUID OZ. (29.5 mL) bottles, UPC 0 11169 20011 8 and b) 1.85 FLUID OZ. (54.5 mL) bottles, UPC 0…

Ecometics, Inc.

FDA Drug Moderate Aug 30, 2023

Rufinamide Tablets, USP 200 mg, packaged in 120-count bottle, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, Ea…

Aurobindo Pharma USA Inc.

FDA Drug Moderate Aug 30, 2023

Helix CBD Therapy Cream (Menthol 7.4%), packaged in a) 3 g pouch (NDC 30775-053-01), b) 2 fl. oz. tubes (NDC 30775-053-02), c) 4 fl. oz. tubes (NDC 3…

Parker Laboratories, Inc.

FDA Drug Moderate Aug 30, 2023

All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.

Inmar Supply Chain Solutions, LLC

FDA Drug Low Aug 30, 2023

Bendamustine HCl Injection, 100mg/4mL (25mg/mL), One 4 mL Multiple-Dose Vial, Rx only, Manufactured for Baxter Healthcare Corporation, Deerfield, IL …

Baxter Healthcare Corporation

FDA Drug Moderate Aug 30, 2023

Semaglutide/Cyanocobalamin 2mg/0.4mg/mL, 1mLvials, Tailor Made Compounding.

TMC Acquisitions LLC dba Tailor Made Compounding

FDA Drug Moderate Aug 30, 2023

NAD+ 200mg/ml, 10ml vials, Tailor Made Compounding.

TMC Acquisitions LLC dba Tailor Made Compounding

FDA Drug Moderate Aug 30, 2023

Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 …

Ecometics, Inc.

FDA Drug Low Aug 30, 2023

Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg, 100-count Bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Aug 30, 2023

Helix CBD Clinical Cream (Menthol 7.4%), packaged in a)3 gm pouches (NDC30775-054-01), b)2 fl. oz. tubes (NDC 30775-054-02), and c) 4 fl. oz. tubes (…

Parker Laboratories, Inc.

FDA Drug Moderate Aug 30, 2023

Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%), packaged in a) 2 fl oz/60 mL Pump bottles (NDC 30775-040-02) and b)18 fl. oz./550 ml Pum…

Parker Laboratories, Inc.

FDA Drug Moderate Aug 30, 2023

YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively, packaged in a) 4 FL OZ (118 mL) bottles, UPC 0 11169 00004 6, and 8 FL OZ …

Ecometics, Inc.

FDA Drug Low Aug 30, 2023

Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075%, 5mL bottle, Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852 …

Imprimis NJOF, LLC

FDA Devices Moderate Aug 30, 2023

Randox Liquid Protein Calibrators-SP CAL-(LIQ)-In vitro diagnostic product used for the calibration of ASO, Complement C3, Complement C4, CRP, Ferrit…

Randox Laboratories Ltd.

FDA Devices Moderate Aug 30, 2023

The Air/Water Valve is provided/used with the following Endoscopes: ULTRASONIC GASTROFIBERSCOPE, ULTRASONIC GASTROVIDEOSCOPE, ULTRASONIC COLONOVIDEO…

Olympus Corporation of the Americas

FDA Devices Moderate Aug 30, 2023

ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP), Material Number 11319151, in vitro diagnostic use in the quantitative determination of t…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Aug 30, 2023

EMBLEM S-ICD Pulse Generator Model A209; Subcutaneous Implantable Cardioverter Defibrillator

Boston Scientific Corporation

FDA Devices Moderate Aug 30, 2023

The O-arm O2 Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and pediatric patients weighing 60 lbs. or…

Medtronic Navigation, Inc.-Littleton

FDA Devices Moderate Aug 30, 2023

IMPIX S, REF numbers: a) B15328071S, b) B15328073S, c) B15328074S, d) B15334072S, e) B15334073S, f) B15334074S; intervertebral fusion de…

Medicrea International

FDA Devices Moderate Aug 30, 2023

IMPIX C+, REF numbers: a) B20240104, b) B20240105, c) B20240106, d) B20240107, e) B20240205, f) B20240206, g) B20240207, h) B20…

Medicrea International

FDA Devices Moderate Aug 30, 2023

BioFire Respiratory Panel 2.1 (RP2.1), REF: 423742, For FILMARRAY systems, IVD, Rx Only

BioFire Diagnostics, LLC

FDA Devices Moderate Aug 30, 2023

IMPIX MANTA, REF numbers: a) A20150407, b) A20250407, c) A20350567, d) B20181743, e) B20181753, f) B20181763, g) B20181773, h) B2018…

Medicrea International

FDA Devices Critical Aug 30, 2023

Carina Sub-Acute Care Ventilator

Draeger Medical, Inc.

FDA Devices Moderate Aug 30, 2023

IMPIX ALIF, REF numbers: a) B15111209, b) B15111212, c) B15111409, d) B15111412; intervertebral fusion device - lumbar

Medicrea International

FDA Devices Moderate Aug 30, 2023

GRANVIA-C, REF numbers: a)¿¿¿¿¿ A13111427, b)¿¿¿¿ A13112567, c)¿¿¿¿¿ A13113456, d)¿¿¿¿ A13131516, e)¿¿¿¿ A13131789, f)¿¿¿¿¿¿ A13132012, …

Medicrea International

FDA Devices Moderate Aug 30, 2023

TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT, REF 71647336, Femur nail

Smith & Nephew, Inc.

FDA Devices Moderate Aug 30, 2023

IMPIX MANTA+, REF numbers: a) B20171743, b) B20171753, c) B20171763, d) B20171773, e) B20171943, f) B20171953, g) B20171963, h) B201…

Medicrea International

FDA Devices Moderate Aug 30, 2023

FilmArray Pneumonia Panel (Pneumo), REF: RFIT-ASY-0145, For FILMARRAY systems, CE 2797, IVD, Rx Only

BioFire Diagnostics, LLC

FDA Devices Moderate Aug 30, 2023

EMBLEM MRI S-ICD Pulse Generator Model A219; Subcutaneous Implantable Cardioverter Defibrillator

Boston Scientific Corporation

FDA Devices Moderate Aug 30, 2023

IMPIX DLIF, REF numbers: a) B16123509, b) B16123511, c) B16124009, d) B16124013, e) B16124509, f) B16124511, g) B16124513, h) B1616…

Medicrea International

FDA Devices Moderate Aug 30, 2023

Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride, Cortisol, Creatinine…

Randox Laboratories Ltd.

FDA Devices Moderate Aug 30, 2023

IMPIX 3D, REF numbers: a) B242C09122810, b) B242C10062810, c) B242C10122810, d) B242C11062810, e) B242C11122810, f) B242C12062810, g)…

Medicrea International

FDA Devices Moderate Aug 30, 2023

TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT, REF 71647340, Femur nail

Smith & Nephew, Inc.

FDA Devices Moderate Aug 30, 2023

IMPIX TLIF, REF numbers: a) B15130607S, b) B15130609S, c) B15130611S, d) B15130613S, e) B15130615S, f) B15900806, g) B15900906, h) B…

Medicrea International

FDA Devices Moderate Aug 30, 2023

DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat. Model Number(s): 1654807 - DOLOMITE GLOSS 680 R…

Invacare Corporation

FDA Devices Moderate Aug 30, 2023

Plum 360 Infusion System, List Numbers: 300100405, 300100409, 300100413, 300100414, 300100415, 300100418, 300100451, 300100452, 300100453, 300100481…

ICU Medical Inc

FDA Devices Moderate Aug 30, 2023

PASS LP, REF numbers: a) B02315535Z, b) B02315540Z, c) B02315545Z, d) B02315550Z, e) B02316535Z, f) B02316540Z, g) B02316545Z, h) B0…

Medicrea International

FDA Devices Moderate Aug 30, 2023

IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar

Medicrea International

NHTSA Critical Aug 30, 2023

VOLKSWAGEN 2019-2020: ELECTRICAL SYSTEM:IGNITION:SWITCH

VOLKSWAGEN

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 July 2026.