PlainRecalls

2025 Recall Year Insight

Federal agencies issued 6,236 product recalls indexed by PlainRecalls in calendar year 2025. That represents about 5.97% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.1 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 125 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 23 critical, 27 moderate, and 0 lower-severity recalls. The page references 14 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Oct 22, 2025

Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W ANGIOGRAPHY PACK MHCA98AK CORONARY ANGIO PACK- 205991 RCAN45C ANGIO CUSTOM RCH UDCO10F CVL CORONARY PACK 219224

American Contract Systems Inc.

FDA Devices Moderate Oct 22, 2025

LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535

GE Medical Systems, LLC

FDA Devices Critical Oct 22, 2025

OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, FJ, (BiD Curve F-J), REF A-TFSE-FJ; cardiac catheter

Abbott

FDA Devices Critical Oct 22, 2025

Model Number U128, VALITUDE CRT-P EL MRI

Boston Scientific Corporation

FDA Devices Critical Oct 22, 2025

BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DD, (BiD Curve D-D), REF A-TFSE-DD; cardiac catheter

Abbott

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Moderate Oct 22, 2025

FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.

Ferno-Washington Inc

FDA Devices Critical Oct 22, 2025

Model Number L231, PROPONENT DR EL MRI Pacemaker

Boston Scientific Corporation

FDA Devices Moderate Oct 22, 2025

TENACIO Pump without InhibiZone; UPN: 72404420;

Boston Scientific Corporation

FDA Devices Critical Oct 22, 2025

BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150

Olympus Corporation of the Americas

FDA Devices Moderate Oct 22, 2025

BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM 18133 BIPOLAR HEAD 41MM 18134 BIPOLAR HEAD 42MM 18135 BIPOLAR HEAD 43MM 18136 BIPOLAR HEAD 44MM 18137 BIPOLAR HEAD 45MM 18138 BIPOLAR HEAD 46MM 18139 BIPOLAR HEAD 47MM 18140 BIPOLAR HEAD 48MM 18141 BIPOLAR HEAD 49MM 18142 BIPOLAR HEAD 50MM 18143 BIPOLAR HEAD 51MM 18144 BIPOLAR HEAD 52MM 18145 BIPOLAR HEAD 53MM 18146 BIPOLAR HEAD 54MM 18147 BIPOLAR HEAD 55MM 181

BioPro, Inc.

FDA Devices Moderate Oct 22, 2025

ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80

Ethicon Endo-Surgery Inc

FDA Devices Critical Oct 22, 2025

EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T180

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

Model Number L101, ESSENTIO DR SL Pacemaker

Boston Scientific Corporation

FDA Devices Moderate Oct 22, 2025

Medical convenience kits Item Number/Description BFCT04X CATARACT PACK - 205986 CMEY17AI EYE PACK - 213187 CMEY17AI EYE PACK - 213187 CMEY17AI EYE PACK - 213187 PERP25AQ PEI RETINAL PACK-206025 RFEY50AC EYE PACK-206026 UIVT47AS VITRECTOMY SUPPLY

American Contract Systems Inc.

FDA Devices Moderate Oct 22, 2025

Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X CYSTO PACK - 205972 IHCY10Y CYSTO PACK MHCY35AE CYSTO PACK- 212487 PLBY52E CYSTO PACK UDCY31Z CYSTO PACK - 206047 UICY28L MOR CYSTO PACK

American Contract Systems Inc.

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Critical Oct 22, 2025

BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100

Olympus Corporation of the Americas

FDA Devices Moderate Oct 22, 2025

Cardiac Workstation 5000; Model Number: 860439;

Philips North America

FDA Devices Moderate Oct 22, 2025

BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/Description: 18593 HEAD FEMORAL 22MM -3 18594 HEAD FEMORAL 22MM +0 19003 HEAD FEMORAL 28MM-6 19004 HEAD FEMORAL 28MM-3 19005 HEAD FEMORAL 28MM+0 19006 HEAD FEMORAL 28MM+3 19007 HEAD FEMORAL 28MM+6 19008 HEAD FEMORAL 28MM+9 19053 HEAD FEMORAL 36MM -3 19054 HEAD FEMORAL 36MM +0 19055 HEAD FEMORAL 36MM +3 19056 HEAD FEMORAL 36MM +6 19057 HEAD FEMORAL 36MM +9 19130 HEAD FEMORAL 32MM-6 19131 HEA

BioPro, Inc.

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Critical Oct 22, 2025

EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, D, (UniD Curve D), REF A-TFSE-D; cardiac catheter

Abbott

FDA Devices Critical Oct 22, 2025

Model Number L209 PROPONENT DR (VDD) SL Pacemaker

Boston Scientific Corporation

FDA Devices Critical Oct 22, 2025

BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170

Olympus Corporation of the Americas

FDA Devices Moderate Oct 22, 2025

Medical convenience kits Item number/ Product description AHLD15X LABOR DELIVERY PACK - 213387 AKDV96B VAGINAL DELIVERY AKDV96B VAGINAL DELIVERY EVBH28D BIRTHING ROOM PACK UPVD01K VAGINAL DELIVERY PACK

American Contract Systems Inc.

FDA Devices Critical Oct 22, 2025

Model Number U226, VISIONIST CRT-P EL

Boston Scientific Corporation

FDA Devices Critical Oct 22, 2025

BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

Percussionaire Corporation

FDA Devices Critical Oct 22, 2025

EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190

Olympus Corporation of the Americas

FDA Devices Moderate Oct 22, 2025

Product: STA Liatest D-Di; REF: 00515;

Diagnostica Stago, Inc.

FDA Devices Moderate Oct 22, 2025

TENACIO Pump with InhibiZone; UPN: 72404429;

Boston Scientific Corporation

FDA Devices Moderate Oct 22, 2025

Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0893-01 Software Version: N/A Product Description: 16 inch DVI-I to DVI-I male/male display cable. Component: Yes, the cable is an external display cable used with the 91390 and 91393

Spacelabs Healthcare, Inc.

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Critical Oct 22, 2025

EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180

Olympus Corporation of the Americas

FDA Devices Critical Oct 22, 2025

PROPONENT SR SL (Model L200)

Boston Scientific Corporation

FDA Devices Critical Oct 22, 2025

Model Number U228, VISIONIST CRT-P EL MRI

Boston Scientific Corporation

FDA Devices Moderate Oct 22, 2025

LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM IP);

Boston Scientific Corporation

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Moderate Oct 22, 2025

Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version: V2025.1.2 Product Description: Intended Use: The ARVIS" system is a computer-controlled navigation system intended to provide intra-operative measurements to the surgeon to aid in selection and positioning of orthopedic implant components. Description: ARVIS Shoulder is a computer-controlled surgical navigation system for shoulder arthroplasty. It aids the s

Kico Knee Innovation Company

FDA Devices Critical Oct 22, 2025

Model Number L221 PROPONENT DR EL Pacemaker

Boston Scientific Corporation

FDA Devices Moderate Oct 22, 2025

Medical convenience kits IHDC30R D AND C PACK

American Contract Systems Inc.

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

FDA Devices Moderate Oct 22, 2025

Basic Biopsy Tray, Item Number NMBP44L

American Contract Systems Inc.

FDA Devices Moderate Oct 22, 2025

Baxter Healthcare Corporation

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2025

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 2025 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.