PlainRecalls

2023 Recall Year Insight

Federal agencies issued 6,706 product recalls indexed by PlainRecalls in calendar year 2023. That represents about 6.42% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 18.4 recalls per day across the FDA, CPSC, USDA FSIS, 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 135 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 10 critical, 35 moderate, and 5 lower-severity recalls. The page references 31 distinct recalling firms operating in 8 distinct product categories, with 39 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), NHTSA (9), FDA Drug (6), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

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 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0 11169 11250 3, Distributed by: Oakhurst Company, Levittown, NY 11756.

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 Ltd. Colvale -Bardez, Goa 403513, India, Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-295-01

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 (NDC 30775-054-04), Parker Laboratories, Inc. 286 Eldridge Road, Fairfield, NJ 07004

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 Pump Bottles (NDC 30775-040-18), Parker Laboratories, Inc. 286 Eldridge Road, Fairfield, NJ 07004

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 (236 mL) bottles, UPC 0 11169 00008 4, The Oakhurst Co., Dist., Levittown, NY 11756.

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 (844)-446-6979, NDC: 71384-311-05.

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, Ferritin, Haptoglobin, IgM, Prealbumin, RF and Transferrin assays Catalogue Number: IT2691

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 COLONOVIDEOSCOPE: GF-UC140P-AL5, GF-UCT140-AL5, GF-UE160-AL5, GF-UCT180, GF-UM20, GF-UM130, GF-UMQ130, GF-UM160, GF-UC160P-OL5, GF-UCT160-OL5

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 total protein in human urine and cerebrospinal fluid

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 greater and having an abdominal thickness greater than 16 cm and is intended to be used where a physician benefits from 2D and 3D information of anatomic structures and objects with high x-ray attenuation such as bony anatomy and metallic objects.

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 device - cervical

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) B20240208; intervertebral fusion device - cervical

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) B20181943, i) B20181953, j) B20181963, k) B20181973, l) B20182253, m) B20182263; intervertebral fusion device - lumbar

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, g)¿¿¿¿¿ B13111014, h)¿¿¿¿ B13111015, i)¿¿¿¿¿¿ B13111016, j)¿¿¿¿¿¿ B13111017, k)¿¿¿¿¿ B13111025, l)¿¿¿¿¿¿ B13111026, m)¿¿¿ B13111027, n)¿¿¿¿ B13111034, o)¿¿¿¿ B13111035, p)¿¿¿¿ B13111036; intervertebral fusion device - cervical

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) B20171973, i) B20172253, j) B20172263, k) B20172273; intervertebral fusion device - cervical

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) B16164009, i) B16164013, j) B16165009, k) B16165013; intervertebral fusion device - lumbar

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, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium, Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems Catalog Number: UC5074

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) B242C12122810, h) B242C12123310, i) B242C13062810, j) B242C13122810, k) B242C14122810, l) B242C15122810, m) B247C07062410, n) B247C07062810, o) B247C07063210, p) B247C08062410, q) B247C08062810, r) B247C08063210, s) B247C09062410, t) B247C09062810, u) B247C09063210, v) B247C10062410, w) B247C10062810, x) B247C10063

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) B15901006, i) B15901106, j) B15901206, k) B15901306; intervertebral fusion device - lumbar

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 ROLLATOR 1655081 - DOLOMITE GLOSS 600 ROLLATOR 1655082 - DOLOMITE GLOSS 520 ROLLATOR 1655083 - DOLOMITE GLOSS 450 ROLLATOR

Invacare Corporation

FDA Devices Moderate Aug 30, 2023

Plum 360 Infusion System, List Numbers: 300100405, 300100409, 300100413, 300100414, 300100415, 300100418, 300100451, 300100452, 300100453, 300100481, 300100483, 300100613, 300101013, 300101113, 300101114, 300101313, 300101379, 300102213, 300102713, 300102913, 300103413, 300103414, 300104213, 300105413, 300105713, 300106313, 300106513, 300106581, 300107813, 300107814, 300108513, 300108813, 300108814, 300109913; infusion pump

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) B02316550Z, i) B02317540Z, j) B02317545Z, k) B02317550Z; intervertebral fusion device - cervical

Medicrea International

FDA Devices Moderate Aug 30, 2023

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

Medicrea International

NHTSA No agency class Aug 30, 2023

VOLKSWAGEN 2019-2020: ELECTRICAL SYSTEM:IGNITION:SWITCH

VOLKSWAGEN

USDA FSIS Critical Aug 29, 2023

Dean & Peeler Meatworks, LLC, Recalls Fresh Ground Beef Products Due to Possible E. Coli O157:H7 Contamination

Dean & Peeler Meatworks

NHTSA No agency class Aug 25, 2023

AUDI 2019-2021: SERVICE BRAKES, HYDRAULIC:FLUID

AUDI

NHTSA No agency class Aug 25, 2023

MACK 2015-2023: EXTERIOR LIGHTING:TURN SIGNAL

MACK

NHTSA No agency class Aug 25, 2023

HYUNDAI 2024: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION:FRONT PASSENGER

HYUNDAI

NHTSA No agency class Aug 25, 2023

FORD,LINCOLN 2018-2023: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

FORD,LINCOLN

NHTSA No agency class Aug 25, 2023

FORD 2023: ENGINE AND ENGINE COOLING:ENGINE:GASOLINE:TURBO/SUPERCHARGER

FORD

NHTSA No agency class Aug 25, 2023

FORD 2023: EXTERIOR LIGHTING:HEADLIGHTS

FORD

NHTSA No agency class Aug 25, 2023

FORD 2023: POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT

FORD

USDA FSIS Moderate Aug 25, 2023

FSIS Issues Public Health Alert for Wegmans Jamaican Jerk Style Chicken Products Due to Misbranding and Undeclared Allergens

Wegmans Food Markets

USDA FSIS Moderate Aug 25, 2023

FSIS Issues Public Health Alert for Shoprite Brand Bowl & Basket Chicken Noodle Soup Due to Misbranding and Undeclared Allergens

Kettle Cuisine Midco, LLC

CPSC No agency class Aug 24, 2023

Aiper Elite Pro Cordless Robotic Pool Vacuum Cleaners Recalled Due to Burn and Fire Hazards; Distributed by Shenzhen Aiper Intelligent Co. (Recall Alert)

Compurobot Technology Company, of China

CPSC No agency class Aug 24, 2023

Multi-Purpose Kids Bike Helmets Recalled Due to Risk of Head Injury, Failure to Meet Bicycle Helmet Standard Requirements; Sold by Ecnup Exclusively on Amazon.com (Recall Alert)

ECNUP, of China

NHTSA No agency class Aug 24, 2023

KIA 2016-2018: LATCHES/LOCKS/LINKAGES:TRUNK LID:LATCH

KIA

FDA Food Moderate Aug 23, 2023

Trader Joe's Fully Cooked Falafel Heat & Eat NET WT. 12 OZ (340g) Distributed and Sold Exclusively By: Trader Joe's Monrovia, CA 91016 UPC 0093 9355

California Ranch Food Company, Inc.

FDA Food Low Aug 23, 2023

Ruxton Chocolates Manning Brand Pumpkin Creme Cookies 19.5 oz. Bulk product packaged in bags, 12 bags per case.

Commercial Bakeries

FDA Food Low Aug 23, 2023

Dilettante Mocha Cafe brand L'Orange Dark Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores contains correct label: "***Dilettante Mocha Cafe L'Orange Dark Bulk Truffles*** UPC 10083 15048***Contains: Milk***Dilettante Mocha Cafe, Tukwila, WA 98188, dilettantemochacafe.com"

Dilettante Chocolates Inc

FDA Food Moderate Aug 23, 2023

VEROCCA, Locally Handmade, ALFAJOR

Daily Meals Corp

FDA Food Low Aug 23, 2023

Dilettante Mocha Cafe brand Sriracha Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores contains correct label: "***Dilettante Mocha Cafe Sriracha Bulk Caramels*** UPC 10083 15055***Contains: Milk***Dilettante Mocha Cafe, Tukwila, WA 98188, dilettantemochacafe.com"

Dilettante Chocolates 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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2023

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2023 across the FDA, CPSC, USDA FSIS 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 September 2026.