PlainRecalls

2025 Recalls

6,168 recalls · Page 78 of 124

2025 Recall Year Insight

Federal agencies issued 6,168 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 6.06% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 16.9 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 124 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 2025.

On this page of 50 records, severity classification shows 2 critical, 47 moderate, and 1 lower-severity recalls. The page references 20 distinct recalling firms operating in 5 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (41), FDA Drug (7), FDA Food (2), 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 2025 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 Jun 4, 2025

Kraft package is labeled as Hummingbird Organic Roasted Salted Cashews, net wt. 6oz.

Honey Heaven Wholesale Inc

FDA Food Critical Jun 4, 2025

Mauna Loa Dark Chocolate Covered Macadamias product is a snack product and packaged in 0.6oz and 4oz plastic flexible pouch. Dist. By Mauna Loa Macad…

HAWAIIAN HOST CANDIES OF LA INC

FDA Drug Moderate Jun 4, 2025

Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals I…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jun 4, 2025

Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals …

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jun 4, 2025

Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited. Colval…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jun 4, 2025

Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC 68462-162-01), b.) 500-count bottle (NDC 68462-162-05), Rx Only, Manufactured by: G…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jun 4, 2025

Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only, Manufactured by: Glenmark Ph…

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Jun 4, 2025

Bromfenac Ophthalmic Solution 0.09%, 1.7 mL bottle, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Man…

Alembic Pharmaceuticals Limited

FDA Drug Critical Jun 4, 2025

ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N

EnShiShiXiangNiShangMaoYouXianGongSi

FDA Devices Moderate Jun 4, 2025

Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " SKU # 70-1071-SRG0266 UDI code: +D7457071SRG02660/$$76254798/16D20250219V The Glidewell HT" Implan…

Prismatik Dentalcraft, Inc.

FDA Devices Moderate Jun 4, 2025

DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)

Pro-Med Instruments Gmbh

FDA Devices Low Jun 4, 2025

Apo B Reagent, REF: OSR6143

Beckman Coulter Ireland, Inc.

FDA Devices Moderate Jun 4, 2025

SEKISUI DIAGNOSTICS LLC SERUM HCG OSOMGENZME CONTROL SET.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

ABBOTT POINT OF CARE TEST CREA I-STAT (25/BX) ABBTPT CARTRIDGE.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

a. Segmental Stem, Cemented, Straight, 100MM, 1 EACH; Model Numbers: CS-09100-03M, CS-10100-03M. b. Segmental Stem, Cemented, Straight, 120MM, 1 E…

Onkos Surgical, Inc.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC ANTI-B BIOCLONE 10ML3X10ML.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Ethos Collar Stem, Cemented, Fluted, 100MM, 1 EACH. Model Numbers: HC-09100-03M, HC-10100-03M, HC-11120-03M, HC-13120-03M, HC-15120-03M, HC-17120-03M…

Onkos Surgical, Inc.

FDA Devices Moderate Jun 4, 2025

VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges, of 18 slides per cartridge, for a total of 90 slides.

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN (60/CR 5CR/PK) ORCLNL REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

BioFire Respiratory Panel 2.1 plus Kit, REF: 423740, For Filmarray systems

BioFire Diagnostics, LLC

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCH AUSAB ANTI-HBS (100/EA) REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Segmental Stem, Canal Filling, Straight, 120MM, 1 EACH. Model Numbers: FS-11120-03M, FS-12120-03M, FS-13120-03M, FS-14120-03M, FS-15120-03M, FS-16120…

Onkos Surgical, Inc.

FDA Devices Moderate Jun 4, 2025

Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by vehicle.

Maquet Cardiopulmonary Ag

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT FREE T4ABBDIA CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs

Cardinal Health 200, LLC

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC ANTI-TPO ASSAY 100TST B REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning system

Ultra Clean Systems, Inc.

FDA Devices Moderate Jun 4, 2025

ABBOTT RAPID DX N AMERICA LLC, TEST CHOLESTEC LDXLIPID PROFILE (10/BX 50BX/CS) CASSETTES.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC GLUC AQUEOUS 1HI/LO HEMCUE CONTROL KIT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS CALCIUM (L-SEQUESTER) (300/PK) REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC CARBON DIOXIDE6X5ML B CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

BD MICROBIOLOGY FLUID THIOGLYCOLLATE MED TUBE 1004321196 (100/CT) MEDIA.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E100436, P3700E100437, P3700E100438…

Baxter Healthcare Corporation

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT HBSAG ASSAY(100TST/BX) BDS REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC HEMOTROL LOW 2X1ML LEVEL 1 HEMCUE CONTROL.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen

Cardinal Health 200, LLC

FDA Devices Moderate Jun 4, 2025

ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARC T-UPTAKE ASSAY (100TST/BX) ABBDIA REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Brand Name: Catalyst+ Product Name: C4D software used in conjunction with Catalyst (SP001-0025), Catalyst HD (SP001-0026), Catalyst PT (S…

C-RAD POSITIONING AB

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC F/GLUCOSE 201 ANALYZER (25/VL 4VL/BX) MICROCUVETTE.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ARCHITECT VITAMIND 6LEVEL CALIBRATOR.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

HEMOCUE INC HEMOTROL HIGH 2X1ML LEVEL 3 HEMCUE CONTROL.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

ORTHO CLINICAL DIAGNOSTICS INC VITROS PHOSPHORUS (60/CR 5CR/PK) ORCLNL REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen

Cardinal Health 200, LLC

FDA Devices Moderate Jun 4, 2025

ABBOTT DIAGNOSTICS ALINITY I FREE PSA US(200TEST/EA) REAGENT.

Mckesson Medical-Surgical Inc. Corporate Office

FDA Devices Moderate Jun 4, 2025

GM Helix Acqua Implant, Article Number: 140.984

Straumann USA LLC

FDA Devices Moderate Jun 4, 2025

NxStage PureFlow-B Solution. Catalog numbers: RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-406, RFP-453, RFP-454, RFP-456.

NxStage Medical Inc

FDA Devices Moderate Jun 4, 2025

Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen

Cardinal Health 200, LLC

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2025 with 2024 →

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 2025

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 2025 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.