Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

8701–8725 of 89535

SevereFDA (Food)·F-0400-2025·2025-01-22
Cucumbers sold in multiple states recalled due to Salmonella contamination risk
Wholesale Produce Supply is recalling cucumbers sold in multiple Midwest states and Canada due to potential Salmonella contamination. Consumers should not eat the affected product and should dispose of it safely.
Product
Cucumbers, Wholesale Produce Supply, 752 Kasota Circle, Minneapolis, MN 554145. Product of Mexico. Cucumbers sold in the following pack sizes: 1. 5 lb. pack 2. 6 ct individual items per case. 3. 12 ct individual items per case. 4. 24 ct individual items per case. 5.
Category
Food
Distribution
9 states
SevereFDA (Devices)·Z-0829-2025·2025-01-22
Impella RP Heart Pump Recalled Due to Optical Sensor Damage Risk
Abiomed is recalling 1,560 units of the Impella RP with SmartAssist pump due to risk of optical sensor damage from device interactions. Damaged sensors may cause temporary or permanent pump malfunction.
Product
Impella RP with SmartAssist; Product Number: 0046-0035;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0905-2025·2025-01-22
Olympus MAJ-891 Forceps Recalled for Potential Biomaterial Retention During Reprocessing
Olympus recalls the MAJ-891 endoscope forceps/irrigation plug nationwide because improper reprocessing may leave biomaterial inside the device, creating a contamination risk.
Product
Olympus MAJ-891 Forceps/Irrigation Plug (Isolated Type). Model/Catalog Number: MAJ-891. This instrument is designed to be attached to the instrument channel port of Olympus endoscopes to allow both irrigation and the use of endo-therapy accessories.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0821-2025·2025-01-22
Neo-Tee Resuscitator Spring Defect May Impair Pediatric Ventilation
Mercury Medical is recalling the Neo-Tee T-Piece Resuscitator due to an undersized spring in the circuit flow controller that may prevent reaching proper pressure ranges, potentially impairing emergency ventilation.
Product
Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810, 1050811, 1050814, 1050832, 1050839, 1050840, 1050841, 1050842
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0822-2025·2025-01-22
ACCOLADE DR Pacemakers Recalled for Unintended Safety Mode Activation
Boston Scientific is recalling ACCOLADE DR Pacemakers built before September 2018 due to risk of unintended Safety Mode activation caused by battery impedance issues. The devices may enter Safety Mode during normal telemetry operations.
Product
ACCOLADE DR Pacemaker, SL (Model Number L301), SL MRI (Model Number L311), EL (Model Number L321), and EL MRI (Model Number L331)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0387-2025·2025-01-22
Kroger Deli Fresh Vegetable Tray Recalled for Potential Salmonella
The Kroger Co is recalling Deli Fresh Vegetable Trays that may contain previously recalled cucumbers with potential Salmonella contamination.
Product
DELI FRESH VEGETABLE TRAY MED, 4 lb., packaged in a plastic container with a plastic lid, UPC 11110-99274
Category
Food
Distribution
7 states
SevereFDA (Food)·F-0389-2025·2025-01-22
Boar's Head hummus vegetable platter recalled for Salmonella contamination
Boar's Head hummus platters are recalled because they may contain cucumbers previously recalled for potential Salmonella contamination. Products were distributed across multiple states.
Product
BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a plastic container with a plastic lid, UPC 42421-61545
Category
Food
Distribution
7 states
SevereFDA (Devices)·Z-0826-2025·2025-01-22
CRT-P Pacemakers Recalled for Potential Safety Mode Initiation Risk
Boston Scientific's ACCOLADE Family pacemakers, including VALITUDE CRT-P models, are recalled due to battery impedance defects that could trigger unintended Safety Mode during normal operation.
Product
VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0200-2025·2025-01-22
Systane Lubricant Eye Drops Recalled for Non-Sterility Risk
Alcon Research is voluntarily recalling Systane Lubricant Eye Drops, Ultra PF, due to non-sterility concerns. The recall affects 55,960 boxes distributed nationwide.
Product
Systane Lubricant Eye Drops, Ultra PF, Sterile, 25 Vials (0.7mL Each), Manufactured for: Alcon Laboratories, Inc. Forth Worth, TX 76134
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0399-2025·2025-01-22
Hardies Fresh Foods Cucumbers Recalled for Potential Salmonella Contamination
Hardies Fresh Foods is recalling certain packaged cucumbers distributed in Texas for potential Salmonella contamination. Consumers should not consume affected products.
Product
14019 Cucumber Select 6 CT, 01034 Cucumber Select 5# packaged in polybags Dairyland Produce, LLC
Category
Food
Distribution
1 state
SevereFDA (Devices)·Z-0886-2025·2025-01-22
Welch Allyn Life2000 Ventilator Battery Charger Malfunction Recall
Baxter Healthcare Corporation is recalling Welch Allyn Life2000 Ventilation Systems due to a battery charger malfunction that triggers an alarm and renders the ventilator inoperable.
Product
Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002AP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0426-2025·2025-01-22
Wicklow Gold Cheddar Cheese Recalled for Potential Listeria Contamination
Abbey Specialty Foods is recalling Wicklow Gold Cheddar Tomato & Herb cheese distributed in Massachusetts, Colorado, and Ohio due to potential Listeria monocytogenes contamination.
Product
Wicklow Gold Cheddar Tomato & Herb, 5.2 oz., plastic cryo-vac , 8 packages per case
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-0765-2025·2025-01-22
Medline Fluid Delivery Sets Recalled Due to Assembly Error
Medline Fluid Delivery Sets were incorrectly assembled with macro drip chambers instead of required micro drip chambers. The macro chamber delivers three times more fluid per drop, creating a risk of dosing errors.
Product
Medline Fluid Delivery Set with Drip Chamber: 1) MTO,135,YELLOW,MICRO,SPK-MAIMONIDES, Item Number: 60130527; 2) MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH, Item Number: 65111341; 3) MTO,ANGIO,SINGLE,SPIKE,KIT, Item Number: 65232486; 4) MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM, Item
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0714-2025·2025-01-22
Endoscopic Access Overtube Recalled for Risk of Obstruction and Pressure Buildup
Trokamed is recalling a 20 Fr. endoscopic access overtube due to risk of obstruction and dangerous kidney pressure buildup during procedures. If inflow speed is too quick, rapid fluid flow can restrict outflow and cause intrarenal pressure to accumulate.
Product
Sheath, 20 Fr., 160 mm (REF: WA2PS20L), gastroenterology-urology endoscopic access overtube.
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-0715-2025·2025-01-22
Endoscopic Access Sheath Recalled Due to Risk of Intrarenal Pressure Buildup
Trokamed GmbH is recalling an endoscopic access sheath (18 Fr., 130 mm) used in gastroenterology and urology. Rapid fluid inflow may block outflow and cause dangerous pressure buildup inside the kidney.
Product
Sheath, 18 Fr., 130 mm (REF: WA2PS18S), gastroenterology-urology endoscopic access overtube.
Category
Medical Device
Distribution
1 state
SevereFDA (Devices)·Z-0885-2025·2025-01-22
Welch Allyn Life2000 Ventilator Battery Charger May Cause Device Inoperability
Baxter Healthcare is recalling 946 Welch Allyn Life2000 ventilators due to a battery charger defect that can trigger an alarm and render the device inoperable.
Product
Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0764-2025·2025-01-22
Medline Fluid Delivery Sets incorrectly assembled with wrong drip chamber
Medline fluid delivery sets were assembled with a macro drip chamber instead of the required micro drip chamber, delivering three times more fluid per drop and risking patient fluid overload.
Product
Medline Fluid Delivery Set with Drip Chamber: 1) FDS,135,CHMN,W/F,MLL,RC(2),PG, Item Number 99000069; 2) FDS,135,NV,MICRO-CHAMBER,W/FILTER,BLUE, Item Number 949000222; 3) FDS,135,NV,MICRO-CHAMBER,W/FILTER,GREEN, Item Number 949000224; 4) FDS,135,NV,MICRO-CHAMBER,W/FILTER,RE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0398-2025·2025-01-22
Daily Veggies Enoki Mushroom Recalled for Possible Listeria Contamination
New Age International recalls Daily Veggies Enoki Mushrooms due to potential Listeria monocytogenes contamination. The product was distributed in New York and Maryland; consumers should not consume it.
Product
Daily Veggies Enoki Mushroom, 200g Product of Korea UPC Codes: 8809159458890
Category
Food
Distribution
2 states
SevereFDA (Food)·F-0393-2025·2025-01-22
Snack Buddies Cucumber Coins Recalled Due to Potential Salmonella Contamination
Snack Buddies Cucumber Coins are being recalled due to potential Salmonella contamination. The affected products were distributed exclusively to California food-service establishments, not retail stores.
Product
Cucumber Coins (sliced cucumbers); 1.25-oz, 2-oz, 2.16-oz, 2.25-oz, 2.6-oz, 3-oz, 4-oz Brand: Snack Buddies
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0837-2025·2025-01-22
Karl Storz Biopsy and Grasping Forceps Recalled Due to Sterility Validation Failure
Karl Storz Endoscopy is recalling 285 units of optical biopsy and grasping forceps (REF 723400) distributed across 31 US states due to failure of manual cleaning validation, which compromises sterility assurance.
Product
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Category
Medical Device
Distribution
32 states
HighFDA (Devices)·Z-0902-2025·2025-01-22
VITROS DGXN Slides Recalled Due to Hemoglobin Interference in Digoxin Measurement
VITROS DGXN Slides are recalled because hemoglobin can interfere with digoxin measurement, producing artificially low results. Approximately 1,541 units were distributed in the US and internationally.
Product
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products DGXN Slides Model/Catalog Number: 8343386 Software Version: Not Applicable Product Description: The VITROS DGXN Slide is a multilayered, analytical element coated on a polyester support. Digoxi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0873-2025·2025-01-22
Intuitive Surgical 8mm Cadiere Forceps Recalled for Frayed Grip Cables
Intuitive Surgical is recalling 56,580 units of the 8mm Cadiere Forceps (Model 471049) due to increased complaints of frayed or broken grip cables on the reusable surgical instrument.
Product
8MM,CADIERE FORCEPS,IS4000 REF 471049
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0849-2025·2025-01-22
Large Needle Driver Surgical Instruments Recalled for Frayed or Broken Grip Cables
Intuitive Surgical recalls 8MM Large Needle Driver instruments (Model 470006) due to frayed or broken grip cables affecting reusable instrument function during surgery.
Product
8MM, LARGE NEEDLE DRIVER, IS4000 REF 470006
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0897-2025·2025-01-22
GE Healthcare Infinia II Systems Detector Fall Risk Recall
GE Healthcare recalls certain Infinia II and related nuclear medicine systems that may have been transported without proper detector support. This risk of detector fall could cause life-threatening bodily injury.
Product
GE Healthcare Infinia II, Model/Catalog Numbers: 1) H2799ZP; 2) H3000WT; System, Tomography, Computed, Emission
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0937-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Surgical Scalpel Handles for Sterile Barrier Risk
Sklar Instruments recalls ECONO STERILE SCALPEL HDL #3 surgical handles due to packaging issues that may compromise the sterile barrier. The 150-unit recall affects units distributed nationwide with lot code SK-125.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCALPEL HDL #3 W/METRIC CS/25, Model Number 96-3500M
Category
Medical Device
Distribution
Distributed nationwide

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8701–8725 of 89535