PlainRecalls

2024 Recall Year Insight

Federal agencies issued 6,264 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 6.00% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.2 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 126 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 2024.

On this page of 50 records, severity classification shows 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 16 distinct recalling firms operating in 4 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (36), FDA Drug (14), 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 2024 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 Dec 11, 2024

Cinacalcet Tablets, 30 mg, 30-count bottle, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 42291-459-30

AvKARE

FDA Drug Moderate Dec 11, 2024

Duloxetine DR Capsules USP 60 mg, a) 30 count (NDC 57237-019-30), b) 90 count NDC 57237-019-90 and c) 1000 count (NDC 57237-019-99) bottles, Distributed by: Rising Pharmaceuticals, Inc., East Brunswick, NJ

Rising Pharma Holding, Inc.

FDA Drug Moderate Dec 11, 2024

Duloxetine Delayed-Release Capsules, USP, 20 mg, Rx only, 60 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For BluePoint Laboratories NDC 68001-413-06

Amerisource Health Services LLC

FDA Drug Moderate Dec 11, 2024

Compliance Dishwashing Liquid & Antibacterial Soap, PCMX 0.1%, Net Contents: 1 Gallon, 128 Ounces, 3.785 Liters, Royal Corporation, 10232 Palm Drive, Santa Fe Springs, CA 90670

Midlab Incorporated

FDA Drug Moderate Dec 11, 2024

Diltiazem Hydrochloride Extended-Release Capsules, USP 60 mg, Twice-a-Day Dosage, Rx Only, 100 Capsules per bottle, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, Product of India, NDC 68462-850-01.

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Dec 11, 2024

Diltiazem Hydrochloride Extended-Release Capsules, USP 60 mg, Twice-a-Day Dosage, Rx Only, 100 Capsules per bottle, Mfd for: Northstar Rx LLC, Memphis, TN, Mfd by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh India, NDC 16714-553-01.

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Dec 11, 2024

Genuine Joe Antibacterial Lotion Soap , Chloroxylenol 0.1%, 1 GALLON (3.78L), Manufactured in the U.S.A. for S.P. Richards Co., Atlanta, GA 30339

Midlab Incorporated

FDA Drug Moderate Dec 11, 2024

Venofer (iron sucrose) Injection, USP 100 mg Elemental Iron per 5 mL (20 mg/mL), 5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, American Regent, Inc. Shirley, NY 11967, NDC: 0517-2340-01 (vial), NDC: 0517-2340-10 (10 x 5 mL/vial cartons), NDC: 0517-2340-25 (25 x 5 mL/vial cartons).

American Regent, Inc.

FDA Drug Moderate Dec 11, 2024

Diltiazem Hydrochloride Extended-Release Capsules, USP 90 mg, Rx Only, 100 Capsules, Manufactured for : Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, Product of India, NDC 68462-851-01.

Glenmark Pharmaceuticals Inc., USA

FDA Drug Moderate Dec 11, 2024

Cinacalcet Tablets, 90 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-833-30), b) 500-count HDPE bottle (NDC 65862-833-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India. 90 mg - 30 Tablets - NDC 65862-833-30 90 mg - 500 Tablets - NDC 65862-833-05

Aurobindo Pharma USA Inc

FDA Drug Moderate Dec 11, 2024

Duloxetine Delayed-Release Capsules USP, 30 mg, a) 30 count (NDC 57237-018-30), b) 90 count (NDC 57237-018-90) and c) 1000 count (NDC 57237-018-99) bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ

Rising Pharma Holding, Inc.

FDA Drug Moderate Dec 11, 2024

MAXIM Assure Antibacterial, Chloroxylenol 0.1%, Net Contents: One U.S. Gallon (3.78 L), For Industrial and Institutional Use Only, MIDLAB 140 Private Brand Way, Athens, TN 37303

Midlab Incorporated

FDA Drug Moderate Dec 11, 2024

Duloxetine Delayed-Release Capsules USP, 20 mg, 60 count bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ NDC 57237-017-60

Rising Pharma Holding, Inc.

FDA Drug Moderate Dec 11, 2024

Sunitinib Malate Capsules, 25 mg, 28-count bottles, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 42291-902-28

AvKARE

FDA Devices Moderate Dec 11, 2024

Non-ablative Fractional Laser Systems, Model: WFB-01

WINGDERM ELECTRO-OPTICS LTD.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: PORT INSERTION PACK, REF DYNJ81597

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

MEDLINE medical convenience kits labeled as: 1) ACETABULAR PACK-LF, REF DYNJ0572894I; 2) LOCAL BASIC, REF DYNJ34418L; 3) LOCAL BASIC, REF DYNJ34418M; 4) MINI LOCAL, REF DYNJ900287D

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) ANGIO PACK #2, REFDYNJ39185D; 2) CV MINOR CATH LAB PACK, REFDYNJ44997J; 3) PLASTIC PACK, REFDYNJ58409C; 4) GENDER AFFIRMING SURGERY, REFDYNJ66252A; 5) ST CHARLES PORT, REFDYNJ909591

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: L&D MINOR PACK, REF DYNJ82672

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

GE Healthcare Revolution ACE, Model number 6670000-3; X-ray/computed tomography systems

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

GE Healthcare Optima 680 Expert, Model number 6670000; X-ray/computed tomography system

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

GE Healthcare Revolution Eagle, Model Number 5849504-3, X-ray/computed tomography system

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) C-SECTION OR 30 CDS, REF CDS820075V; 2) C-SECTION OR 30 CDS, REF CDS820075W; 3) C-SECTION, REF CDS980774M; 4) C-SECTION KIT, REF CDS981322AB; 5) C-SECTION KIT, REF CDS981322AC; 6) C-SECTION COMBINED CDS, REF CDS982398I; 7) C-SECTION PROCEDURE, REF CDS983450L; 8) C-SECTION-LF, REF CDS983869J; 9) C-SECTION, REF CDS984261J; 10) C-SECTION CDS-LF, REF CDS984516L; 11) C-SECTION CDS-LF, REF CDS984516M; 12) C-SECTION, REF CDS984902K; 13) C-SECTION, R

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: COLON WOUND CLOSURE PACK, REF DYNJ52141B

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) MAJOR VASCULAR-LF, REF CDS840232L; 2) AVF-LF, REF CDS840233I; 3) GENERAL AAA #11-RF, REF CDS840261AB; 4) HEART CDS, REF CDS840387T; 5) OPEN HEART CDS PART A, REF CDS840402AF; 6) OPEN HEART CDS PART A, REF CDS840402AI; 7) HEART PACK, REF CDS840459R; 8) CAROTID-LF, REF CDS860039K; 9) CAROTID-LF, REF CDS860039L; 10) OPEN HEART ADULT KIT, REF CDS981319AD; 11) BAPTIST AAA, REF CDS982400M; 12) ZALE PUMP CDS, REF CDS983187G; 13) PEDIATRIC CARDIAC CD

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK, REF CDS780202P; 2) BASIC NEURO PACK, REF CDS780202Q; 3) BASIC NEURO PACK, REF CDS780202R; 4) ACDF CDS, REF CDS941061M; 5) NEURO KIT, REF CDS981327Q; 6) ZALE V-P SHUNT CDS, REF CDS983186J; 7) NEURO PACK-LF, REF DYNJ0038440C; 8) NEURO PACK-LF, REF DYNJ0406347M; 9) NEURO-LF, REF DYNJ0484186M; 10) NEURO-LF, REF DYNJ0484186N; 11) NEURO VP SHUNT PACK-LF, REF DYNJ0843121K; 12) NEURO VP SHUNT/VAGAL NERVE-RF, REF DYNJ21925

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

GE Healthcare Discovery RT, Model Number 2374681-17, X-ray/computed tomography systems labeled as:

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

Ziehm Solo. Digital Mobile C-arm

Orthoscan, Inc.

FDA Devices Moderate Dec 11, 2024

Ziehm Solo FD. Interventional fluoroscopic x-ray system

Orthoscan, Inc.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) BURN, REF CDS983465M; 2) BURN, REF CDS983465N; 3) BURN PACK, REF DYNJ63331D

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

Ziehm Vision RFD. Interventional fluoroscopic x-ray system

Orthoscan, Inc.

FDA Devices Moderate Dec 11, 2024

Diode Laser Hair Removal model: WLA-01

WINGDERM ELECTRO-OPTICS LTD.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907I; 2) LAKELAND SINGLE BASIN PACK-LF, REF DYNJ0619907K; 3) LKLND SNGL BASIN PK RFID-LF, REF DYNJ0619907L; 4) BASIN SET W/ RING BASIN, REF DYNJ06966M; 5) OPEN HEART C--BASIN PACK-LF, REF DYNJ0867331G; 6) TOTAL KNEE BASIN B PACK-LF, REF DYNJ0867555L; 7) ST. ANNE'S MINOR BASIN PACK, REF DYNJ24622K; 8) ST. ANNE'S MAJOR BASIN SET UP, REF DYNJ24628M; 9) MAJOR BASIN SET, REF DYNJ41285B; 10) BASIN P

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

GE Healthcare Revolution Frontier, Model Numbers: 1) 5232085-213, 2) 5873009; X-ray/computed tomography system

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

GE Healthcare Revolution Advance, Model number 5849504; X-ray/computed tomography systems

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

Atellica CI Analyzer. Catalog Numbers: 10947347.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Dec 11, 2024

BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990

Becton Dickinson & Co.

FDA Devices Moderate Dec 11, 2024

BD Synapsys Informatics Solution (Laboratory Solution) Version or Model: 444150 Catalog Number: 444150

Becton Dickinson & Co.

FDA Devices Moderate Dec 11, 2024

MEDLINE MAXORB EXTRA ALGINATE WOUND DRESSING 4X4 SQUARE REF MSC7044EP MEDLINE MOXORB EXTRA ALBINATE WOUND DRESSING 4X8 RECTANLE REF MSC7048EP Wound dressing indicated for moderate to heavily exuding chronic and acute wounds, and to control minor bleeding in superficial wounds.

Advanced Medical Solutions Ltd.

FDA Devices Moderate Dec 11, 2024

BD MAX System, BD MAX Instrument Version or Model: 441916 Catalog Number: 441916

Becton Dickinson & Co.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY-LF, REF CDS760059I; 2) GYN LAPAROSCOPY CDS #34-RF, REF CDS920099S; 3) GYN MAJOR, REF CDS980998L; 4) ROBOTIC PROCEDURE, REF CDS982128P; 5) ROBOTIC, REF CDS984262N; 6) GYN LAPAROSCOPY, REF CDS984900M; 7) GYN LAPAROSCOPY, REF CDS984900N; 8) DAVINCI PACK-LF, REF DYNJ0101304G; 9) PROSTATE ROBOTIC PACK, REF DYNJ0347372J; 10) URO GYN PACK-LF, REF DYNJ17454N; 11) DB DAVINCI ROBOT PACK-LF, REF DYNJ33592I; 12) ROBOTIC UROLOGY

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

GE Healthcare Revolution Maxima Select, Model Number, 6670000-55; X-ray/computed tomography system

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

GE Healthcare Operator Console Upgrade Types, FRU Spare Parts Number B80212DA: EU: Operator Console (for BrightSpeed, Elite/BrightSpeed Elite Select), Non-EU: BrightSpeed Elite, BrightSpeed Elite Select; X-ray/computed tomography system

GE Healthcare (China) Co., Ltd.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) CIRCUMCISION PACK, REF DYNJ16826O; 2) D-CIRCUMCISION PACK, REF DYNJ64432; 3) PACK,CIRCUMCISION ASC, REF DYNJ906909A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

Hollister CalciCare Calcium Alginate Dressing REF 529937R calcium alginate dressings are indicated for moderate to heavily exuding chronic and acute wounds such as: ¿ pressure ulcers ¿ leg ulcers ¿ cavity wounds ¿ lacerations ¿ post-operative surgical wounds

Advanced Medical Solutions Ltd.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) TRACH TOTE, REF DYNJ85691; 2) TRACHEOSTOMY, REF DYNJ902123J

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.

Smith & Nephew Inc.

FDA Devices Moderate Dec 11, 2024

MEDLINE convenience kits labeled as: 1) TOT/ GYN LITHOTOMY CDS, REF CDS985431J; 2) TOT/ GYN LITHOTOMY CDS, REF CDS985431K; 3) TOT/ GYN LITHOTOMY CDS, REF CDS985431L; 4) GENERAL LITHOTOMY PACK, REF DYNJ44153G; 5) CHRISTUS AH GYN LAPAROSCOPY, REF DYNJ60924C; 6) D&C PACK, REF DYNJVB1280C; 7) D&C PACK, REF DYNJVB1280D

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Dec 11, 2024

Spectral CT and Spectral CT Plus. Model Numbers: 728333, 728340, 728344.

Philips North America Llc

FDA Devices Moderate Dec 11, 2024

BD BACTEC FX, Instrument Top, Packaged Version or Model: 441385 Catalog Number: 441385

Becton Dickinson & Co.

Nearby Recall Years

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

Compare 2024 with 2023 →

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 2024

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 2024 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.