PlainRecalls

2023 Recalls

6,617 recalls · Page 44 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, 43 moderate, and 2 lower-severity recalls. The page references 24 distinct recalling firms operating in 5 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (36), FDA Food (7), NHTSA (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 Moderate Aug 16, 2023

Semolina Roasted Red Pepper Linguine, net wt. 14oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted…

Bellingham Pasta Co

FDA Food Moderate Aug 16, 2023

Semolina Vegan Rigatoni, net wt. 13oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham P…

Bellingham Pasta Co

FDA Food Critical Aug 16, 2023

Cava Spicy Hummus UPC 89832800227 Net Wt. 8oz./226.8 g Packaged in clear plastic container. 12 units per case

Cava Foods LLC

FDA Food Moderate Aug 16, 2023

Sweet Alchemy Blackberry Crumble ice cream, distributed in pints. Label declares company name, flavor name, but does not declare ingredients and all…

Sweet Alchemy Ice Creamery, Inc

FDA Food Moderate Aug 16, 2023

Romaine lettuce packed in bulk 45-lb mini-bins

C&E Farms, Inc.

FDA Food Moderate Aug 16, 2023

Semolina Lemon Black Pepper Linguine, net wt. 14oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted…

Bellingham Pasta Co

FDA Food Moderate Aug 16, 2023

Sweet Alchemy Toasted Black Sesame ice cream, distributed in pints. Label declares company name, flavor name, but does not declare ingredients and al…

Sweet Alchemy Ice Creamery, Inc

FDA Drug Low Aug 16, 2023

Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 19…

SUN PHARMACEUTICAL INDUSTRIES INC

FDA Drug Low Aug 16, 2023

0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018, NDC 0264-5802-00

B. Braun Medical Inc.

FDA Devices Moderate Aug 16, 2023

Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) UR3825 (2) UR3873 (3) UR8334 (4) UR8070 (Modena)

Randox Laboratories Ltd.

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 17 - indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 25 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 14-Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip j…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

ARTIS pheno-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 10849000

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 16, 2023

VITROS Immunodiagnostic Products Troponin I ES Reagent Pack

ORTHO-CLINICAL DIAGNOSTICS

FDA Devices Moderate Aug 16, 2023

Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Olympus Light Source, documentation equipment, display monitor and other ancillary eq…

Olympus Corporation of the Americas

FDA Devices Moderate Aug 16, 2023

CD HORIZON Spinal System Solera Awl Tip Tap, REF NAV2006K

Medtronic Sofamor Danek USA, Inc

FDA Devices Moderate Aug 16, 2023

Total Hip Kit, REF DYNJ903275S; surgical convenience kit

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Aug 16, 2023

Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their access…

Olympus Corporation of the Americas

FDA Devices Moderate Aug 16, 2023

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)

Philips North America

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 22 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

ARTIS icono floor-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 11327700

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 16, 2023

Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their acces…

Olympus Corporation of the Americas

FDA Devices Moderate Aug 16, 2023

Medtronic InterStim Ground Pad REF 041826

Medtronic Neuromodulation

FDA Devices Moderate Aug 16, 2023

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)

Philips North America

FDA Devices Moderate Aug 16, 2023

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)

Philips North America

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 15 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

UroLift Visual Obturator, 20Ch-The visual obturator is used with the UroLift¿ system. Instrument for insertion of a cystoscope shaft into the bladder…

Scholly Fiberoptic Gmbh

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 16 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 19-Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip j…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

ellacor System with Micro-Coring Technology-Indicated for use by medical professionals for the treatment of moderate and severe wrinkles in the mid a…

Cytrellis Biosystems, Inc.

FDA Devices Moderate Aug 16, 2023

MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)

Philips North America

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 21 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway management which includes endoscopic observation to access airway anatomy, endotr…

Olympus Corporation of the Americas

FDA Devices Moderate Aug 16, 2023

Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106

Philips North America

FDA Devices Moderate Aug 16, 2023

INFX-8000C XGCP-930AA TABLE SIDE CONSOLE, INFX-8000C XGCP-930BA TABLE SIDE CONSOLE

Canon Medical System, USA, INC.

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 18 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 24 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 20 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106

Philips North America

FDA Devices Moderate Aug 16, 2023

ARTIS icono biplane -Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 11327600

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 16, 2023

LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 23 - Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip…

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Aug 16, 2023

Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accesso…

Olympus Corporation of the Americas

FDA Devices Moderate Aug 16, 2023

VITROS Immunodiagnostic Products Troponin I ES Calibrators

ORTHO-CLINICAL DIAGNOSTICS

FDA Devices Moderate Aug 16, 2023

HoverMatt, 39" W x 78" L, REF: HM39SPU-B

Stryker Sustainability Solutions

CPSC Moderate Aug 16, 2023

Gree Recalls 1.56 Million Dehumidifiers Due to Fire and Burn Hazards; Reports of At Least 23 Fires

Gree Electric Appliances, Inc. of Zhuhai

NHTSA Critical Aug 16, 2023

BMW 2019-2022: SEAT BELTS

BMW

NHTSA Critical Aug 15, 2023

NISSAN 2020-2022: STEERING:LINKAGES:TIE ROD ASSEMBLY

NISSAN

NHTSA Critical Aug 15, 2023

KIA 2023: EQUIPMENT:OTHER:LABELS

KIA

NHTSA Critical Aug 14, 2023

JEEP 2021-2024: BACK OVER PREVENTION:DISPLAY FUNCTION

JEEP

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.