PlainRecalls

2026 Recall Year Insight

Federal agencies issued 3,961 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 3.79% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 10.9 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 80 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 2026.

On this page of 50 records, severity classification shows 0 critical, 48 moderate, and 2 lower-severity recalls. The page references 18 distinct recalling firms operating in 5 distinct product categories, with 36 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (28), FDA Drug (22), 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 2026 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 Jan 21, 2026

EXCEDRIN 2'S DISP.- 30 CT

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGATE, MAXFRESH, SPICY FRESH, RED TOOTH PASTE, 72CT, 150G; e) CREST, TOOTHPASTE, 40CT, 8.2OZ, UPC: 037000247081

GOLD STAR DISTRIBUTION INC

FDA Drug Low Jan 21, 2026

Fluocinolone Acetonide Solution Topical Solution USP, 0.01%, 60-mL bottles, Rx only, Dist. by: Taro Pharmaceuticals Inc., Hawthorn, NY 10532. NDC 51672-1365-4

SUN PHARMACEUTICAL INDUSTRIES INC

FDA Drug Moderate Jan 21, 2026

Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz, UPC: 048155921092; e) AXE, BODY SPRAY, APOLLO, 6CT, 150ML; f) AXE, BODY SPRAY, BLACK, 6CT, 150ML; g) AXE, BODY SPRAY, DARK TEMPTATION, 6CT, 150ML; h) AXE, BODY SPRAY, GOLD, 6CT, 150ML; i) AXE, BODY SPRAY, EXCITE, 6CT, 1

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Halls Cough Drops a) BAGS, MENTHOL, 12CT; b) BAGS, HONEY LEM, 12CT; c) BAGS, DEFENSE CITRUS, 12CT; d) BAGS, CHERRY, 12CT; e) M. CHERRY, 20 STK; f) BRAZIL, Cherry, 21CT/27.5G; f) LEMON. HONEY, 20CT #1180E; g) LIME FRESH, 20CT, #1182; h) MENTHOL BLUE, 20CT, #1180A; i) BRAZIL, Menthol, 21CT/27.5G, j) M . STRAWBERRY, 20 STK; k) DEFENSE, VITAMIN C, 20CT, #1181

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

PEPTO BISMOL 32CT

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

AQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each

Encon Safety Products Co

FDA Drug Moderate Jan 21, 2026

LIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67

Cipla USA, Inc.

FDA Drug Moderate Jan 21, 2026

NYQUIL COLD & FLU -32CT/2PK

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Claritin, 20 Count, UPC: 655708016305

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

TESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets per carton, Rx only, Manufactured by: Advanced Pharmaceutical Technology, 132 South Central Avenue, Elmsford, NY 10523, NDC# 57377-100-01

Advanced Pharmaceutical Technology, Inc.

FDA Drug Moderate Jan 21, 2026

Levothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10.

Alvogen, Inc

FDA Drug Moderate Jan 21, 2026

Bayer 2Pk- 25 CT

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

PEPCID COMPLETE - 25CT

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

DAYQUIL COLD & FLU, 32CT/2PK

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932

GOLD STAR DISTRIBUTION INC

FDA Drug Moderate Jan 21, 2026

Benadryl, 25'S 2PK Box, UPC 815556020316

GOLD STAR DISTRIBUTION INC

FDA Drug Low Jan 21, 2026

Clindamycin Phosphate USP, 1% (10 mg/mL), Topical Solution, 60 mL per applicator bottle, Rx only, Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel; Dist. by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC# 51672-4081-4

SUN PHARMACEUTICAL INDUSTRIES INC

FDA Devices Moderate Jan 21, 2026

MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO)

Elekta, Inc.

FDA Devices Moderate Jan 21, 2026

VANTAGE GALAN 3T Model MRT-3020/MEXL-3020

Canon Medical System, USA, INC.

FDA Devices Moderate Jan 21, 2026

Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box)

Intuitive Surgical, Inc.

FDA Devices Moderate Jan 21, 2026

BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F

HANGZHOU BEVER MEDICAL DEVICES CO., LTD.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10F; Model Number: 722002;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ54488A

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Brand Name: PALACOS Product Name: PALACOS R+G pro 40; PALACOS R+G pro 80 Model/Catalog Number: 5081288; 5081289 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A

Heraeus Medical GmbH (Dental Division)

FDA Devices Moderate Jan 21, 2026

A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).

Medtronic Neuromodulation

FDA Devices Moderate Jan 21, 2026

Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174

Medicrea International

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B; 2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B; 3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C; 4) TOP DRAWER #6, Medline kit SKU ACC010688; 5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770; 6) SURGERY BAG, Medline kit SKU DYKM1279C; 7) ADMISSION KIT, Medline kit SKU DYKS1179; 8) PRE OP KIT, Medline kit

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10/10; Model Number: 722027;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20; Model Number: 722028;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Product Name: Allura Xper FD10C; Model number: 722001;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5. Azurion 7 B12. Model Number: 722235. 6. Azurion 7 B20. Model Number: 722236. 7. Azurion 7 M12. Model Number: 722233. 8. Azurion 7 M20. Model Number: 722234.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10; Model Number: 722003;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE, REF CDS980754T; 2) GYN LAP HYSTERECTOMY CDS, REF CDS982662Q; 3) DAVINCI HYSTERECTOMY CDS, REF CDS985344F; 4) LAVH, REF DYNJQ9041R; 5) LAPAROSCOPIC HYSTERECTOMY, REF DYNJ900244I; 6) ROBOTIC LAVH, REF DYNJ901281I; 7) LAVH-LF, REF DYNJ901829T; 8) LEX LAP HYST, REF DYNJ902030J; 9) LITHOTOMY-SLINGS-LF, REF DYNJ905274D; 10) GYN LAPAROSCOPY, REF DYNJ905485J; 11) ROBOTIC HYSTERECTOMY, REF DYNJ906380C; 12)

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) PRE OP KIT, Medline kit SKU DYKS1093B; 2) PRE OP KIT, Medline kit SKU DYKS1124C; 3) PRE OP KIT, Medline kit SKU DYKS1128C; 4) PREOP KIT, Medline kit SKU DYKS1130B; 5) PRE OP KIT, Medline kit SKU DYKS1163G; 6) PRE OP KIT SURGERY, Medline kit SKU DYKS1263G; 7) PREOP KIT, Medline kit SKU DYKS1313A; 8) PRE OP KIT, Medline kit SKU DYKS1325A; 9) ADULT PRE OP KIT, Medline kit SKU DYKS

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.

Mobius Imaging, LLC

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10/10; Model Number: 722011;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

MAVERICK¿ Measurement Module Spectrometer PN 820-01367 (originally part of a kit PN 820-01519) Finished Goods PN 820-01496

REPLIGEN CORPORATION

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20/20; Model Number: 722038;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B

Medline Industries, LP

FDA Devices Moderate Jan 21, 2026

Allura Xper FD10/10; Model Number: 722005;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Allura Xper FD20; Model Number: 722012;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Jan 21, 2026

Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG

ICU Medical Inc.

FDA Devices Moderate Jan 21, 2026

Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF, REF CDS860235L; 2) GENERAL LAPAROSCOPIC, REF CDS930223M; 3) LAP CHOLE CDS, REF CDS983678K; 4) LAPAROSCOPY PELV CDS, REF CDS983679K; 5) LAP CHOLE CDS-LF, REF CDS983752M; 6) LAP CHOLE CDS-LF, REF CDS984016B; 7) LAP CHOLE KIT, REF CDS984020P; 8) LAP CHOLE-LF, REF CDS984175J; 9) LAP COLON CDS, REF CDS984849N; 10) GENERAL LAPAROSCOPY CDS, REF CDS985328M; 11) LAP CHOLE, REF DYNJQ9044O; 12) GENERAL LA

Medline Industries, LP

Nearby Recall Years

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

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 2026

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 2026 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.