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Consumer Product Recalls

127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.

September 24, 2025Medical DevicesFDA
BigTree Sales Inc. recalls The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emissi
Hazard: The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons.
September 24, 2025Medical DevicesFDA
Philips Medical Systems (Cleveland) Inc recalls Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code: (01)008
Hazard: Due to a software issue, there is a potential image error of the Region of Interest for expansion/contraction for HFP (Head First Prone), FFS (Feet First Supine) and FFP (Feet First Prone) orientations.
September 24, 2025Medical DevicesFDA
Medical Information Technology, Inc. recalls MEDITECH Expanse Laboratory (LAB), Microbiology (MIC), Anatomical Pathology (PTH), Genetics (GEN). Calculator/data proce
Hazard: Entering multiple keys that trigger input simultaneously may remove data from first field of screens and/or questionnaires with more than one field.
September 24, 2025Medical DevicesFDA
Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461
Hazard: Their is the potential for weak staining which may result in false negative CD20 identification.
September 24, 2025Medical DevicesFDA
Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461
Hazard: Their is the potential for weak staining which may result in false negative CD20 identification.
September 24, 2025Medical DevicesFDA
Agilent Technologies Denmark ApS recalls Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461
Hazard: Their is the potential for weak staining which may result in false negative CD20 identification.
September 24, 2025Medical DevicesFDA
Exactech, Inc. recalls Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE 38MM HUM LINER +0), REF: 322-38-03 (145-DEG
Hazard: Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.
September 24, 2025Medical DevicesFDA
Exactech, Inc. recalls Exactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE
Hazard: Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.
September 24, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slides, for a
Hazard: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencing an increased occurrence of calibration failure related to lots from coating 0130 and above with Condition Code TH4-63J during calibration, causing the delay of lac test results and potentially impact patient management. The issue was identified by QuidelOrtho through an increase in customer complaints compared to the historical baseline with average failure rate of 1% for coating 0130 in 2025 while average of failure rate for other coating was 0.06% in 2025 and average of failure rate for all coatings is 0.03% for 2024.
September 24, 2025Medical DevicesFDA
Ortho-Clinical Diagnostics, Inc. recalls Chemistry Products LAC Slides. Catalog Number: 8433880. 1 Sales Unit = contains 5 cartridges of 60 slides, for a total o
Hazard: VITROS Chemistry Products LAC Slides on VITROS XT 3400 and VITROS XT 7600 Systems are experiencing an increased occurrence of calibration failure related to lots from coating 0130 and above with Condition Code TH4-63J during calibration, causing the delay of lac test results and potentially impact patient management. The issue was identified by QuidelOrtho through an increase in customer complaints compared to the historical baseline with average failure rate of 1% for coating 0130 in 2025 while average of failure rate for other coating was 0.06% in 2025 and average of failure rate for all coatings is 0.03% for 2024.
September 24, 2025Medical DevicesFDA
Boston Scientific Neuromodulation Corporation recalls Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09
Hazard: Wire break(s) have occurred in rechargeable deep brain stimulation implantable pulse generators, implanted in the submuscular pectoral location. Wire breaks prevent successful stimulation, thus requiring device removal/replacement and users may experience high monopolar impedances, undesired sensation, loss of therapy, return of symptoms and/or Bluetooth connectivity challenges.
September 24, 2025Medical DevicesFDA
Max Mobility LLC recalls Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Whe
Hazard: Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
September 24, 2025Medical DevicesFDA
Max Mobility LLC recalls Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Whee
Hazard: Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
September 24, 2025Medical DevicesFDA
Max Mobility LLC recalls Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheel
Hazard: Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
September 24, 2025Medical DevicesFDA
3M Company recalls 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
Hazard: Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.
September 24, 2025Food & BeverageFDA
Itacate Foods LLC recalls CAMPSITE LENTEJAS Hearty lentil soup with a tomato and cilantro base that takes no time to rehydrate. NET WT 4.0 OZ (115
Hazard: Undeclared Yellow #5 and Yellow #6.
September 24, 2025Food & BeverageFDA
Itacate Foods LLC recalls CHARGE-UP CHILAQUILES Traditional Mexican breakfast consisting of tortilla chips smothered in a spicy tomatillo salsa an
Hazard: Undeclared Yellow #5 and Yellow #6.
September 24, 2025Food & BeverageFDA
I C F Factory Inc recalls Vanilla G. Nutt Ice Cream (pint, quart, or half gallon)
Hazard: May contained undeclared almond
September 24, 2025Food & BeverageFDA
E&E Foods Inc recalls Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum Package
Hazard: Goldband Snapper is recalled because testing confirmed fish is Sharptooth Snapper.
September 24, 2025Food & BeverageFDA
HARD EIGHT NUTRITION LLC recalls Brand name: BulkSupplements.com Generic name: Inositol. Dosage: 1 gram. Form: Powder. Route of administration: Oral. Pac
Hazard: Finished product possibly contaminated with pathogenic Staphylococcus aureus.
September 24, 2025Food & BeverageFDA
Endico Potatoes Inc recalls Endico brand PEAS & CARROTS; NET WT. 2.5 lbs (40 oz.) (1134 g); KEEP FROZEN UNTIL READY TO USE; Dist. by Endico Potatoes
Hazard: Product may be contaminated with Listeria monocytogenes.
September 24, 2025Food & BeverageFDA
Endico Potatoes Inc recalls Endico brand MIXED VEGETABLES; NET WT. 2.5 lbs (40 oz.) (1134 g); KEEP FROZEN UNTIL READY TO USE; Dist. by Endico Potato
Hazard: Product may be contaminated with Listeria monocytogenes.
September 24, 2025Food & BeverageFDA
Fresh & Ready Foods LLC recalls Chili Crunch Market Mezze; Keep Refrigerated, NET WT: 14.5 OZ, UPC# Manufactured by Fresh and Ready Foods LLC, San Fer
Hazard: undeclared allergen (Wheat) on ready to eat sandwiches.
September 24, 2025Food & BeverageFDA
Fresh & Ready Foods LLC recalls Piccolo Pranzo Box; Keep Refrigerated, NET WT: 14.5 OZ, UPC# Manufactured by Fresh and Ready Foods LLC, San Fernando,
Hazard: undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
September 24, 2025Food & BeverageFDA
Fresh & Ready Foods LLC recalls Tuscan Artichoke and Mozzarella Salad; Keep Refrigerated, NET WT: 8.5 OZ, UPC# 6 82906 90935 1 Manufactured by Fresh an
Hazard: undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
September 24, 2025Food & BeverageFDA
Fresh & Ready Foods LLC recalls Spanish Club Ciabatta; Keep Refrigerated, NET WT: 10.5 OZ, UPC# 6 82906 90933 7 Manufactured by Fresh and Ready Foods L
Hazard: undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
September 24, 2025Food & BeverageFDA
Wang Globalnet recalls (Bulk) Oyster, Frozen, Raw Half Shell, 15lb(6.8kg) UPC: 10087703078342 Harvest Dates: Jan 03,2025, Jan 14,2025
Hazard: Oyster product potentially contaminated with Norovirus
September 24, 2025Food & BeverageFDA
PRIMO NO. 1 IN PRODUCE, INC recalls Cucumber Sliced 8oz 8ct/4#AV, Cardboard Boxes
Hazard: Product contaminated with Salmonella
September 24, 2025Food & BeverageFDA
PRIMO NO. 1 IN PRODUCE, INC recalls Vegetable Tray Cucumbers 3/2lb, Cardboard boxes
Hazard: Product contaminated with Salmonella
September 24, 2025Food & BeverageFDA
PRIMO NO. 1 IN PRODUCE, INC recalls Cucumber Sliced PLD ¿ KBS 2/10lb, Cardboard Boxes
Hazard: Product contaminated with Salmonella