cpsc regulated Recalls

2,142 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DEVICE

Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)

Ion Beam Applications S.A. recalled four PROTEUS 235 proton therapy systems distributed worldwide, including Florida in the United States, and the countries of Italy and Japan. The defect disables the Therapy Safety System's Universal Beam Triggering Interface, so the system may not stop beam delivery if the Healthy Signal from an external gating device is lost. Patients and healthcare providers应该

Ion Beam Applications
It was
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Food & Beverages
HIGH
FDA FOOD

Pure Solutions Recalls Sleep Formula Over Milk Allergen Risk

Pure Solutions recalled 442 bottles of its sleep supplements on February 3, 2026. The labels did not declare a milk allergen despite containing bovine colostrum. Consumers should stop using the product immediately and seek refunds.

Pure Solutions
Label declares
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe Core Instrument Kit KIT-311X Recalled for Missing Cross-Pin

Exactech recalls 596 Equinoxe Core Instrument Kit units due to a missing cross-pin on the impacter handle. The alert, categorized as a Class II recall, was issued Feb 3, 2026 and remains active. Affected kits were distributed across the United States and in multiple international markets. Stop using the device and follow manufacturer instructions for recall remedies.

Exactech
Impactor handle
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Health & Personal Care
HIGH
FDA DRUG

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Violations

Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.

PRO NUMB SENSITIVE SKIN
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 21GA Winged Infusion Set (7A3842) 21,000 Units (2026)

B. Braun Medical is recalling 21,000 21GA Winged Infusion Sets (Single Pack) distributed worldwide, including Texas and Costa Rica, catalog 7A3842. The needle tip can be dull or blunt, may be difficult to advance, or break. Clinicians and patients should stop using the device and await manufacturer instructions.

B. Braun Medical
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Tandem Diabetes Care Insulin Infusion Pumps Recalled 1,380 Units in 2026 Over Czech Guide Error

Tandem Diabetes Care recalled 1,380 insulin infusion pumps distributed internationally in the Czech Republic and Slovakia after translation errors in the Czech user guide could cause unintended insulin delivery. The most significant error told users to verify the infusion set is connected to the body when it should be confirming it is not connected. Following this instruction could result in a hyp

Tandem Diabetes Care
The Czech
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 780G Recall 2026: 26,851 Pumps Hit Over Software Defects

Medtronic MiniMed recalled 26,851 MiniMed 780G insulin pumps sold worldwide, including the United States and Israel. Three software defects tied to updates 6.60, 6.61, and 6.62 could misdose insulin. Stop using the affected pumps and follow the recall letter for instructions.

Medtronic MiniMed
Three software
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter AU5800 Chemistry Analyzer Recall for 47 Units Over Calibration Delay Issues (2026)

Beckman Coulter Mishima K.K. recalled 47 AU5800 chemistry analyzers sold nationwide in the United States after a software delay can cause calibration and reagent databases to fail to open. The issue occurs when a calibration monitor using Microsoft SQL Server 2022 Express remains open for more than 15 minutes, potentially halting analysis. Healthcare facilities should stop using the devices and (a

Beckman Coulter
A delay
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Health & Personal Care
HIGH
FDA DEVICE

Medline Chest Drainage Units Recall Updated IFUs for Adults 18+

Medline Industries recalls 2,894 Aqua-Seal Chest Drainage Units from Cardinal Health after updating IFUs to specify adult patients 18 years and older. The devices were distributed worldwide, including California, Chile and Panama. The update clarifies intended patient population and requires action from healthcare providers to stop use until further notice.

Medline Industries, LP
The instructions
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Food & Beverages
HIGH
FDA FOOD

Reser's Tuna Salad Recalled Over Undeclared Fish Allergen

Reser's Fine Foods recalled 298 tubs of Tuna Salad on January 30, 2026 due to undeclared fish allergens. The product was mislabeled with a Chicken Salad lid, posing a risk to consumers with fish allergies. The recall affects distribution in Arizona, California, Nevada, Utah, and Washington.

Reser's Fine Foods
Undeclared fish
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Recalled Teether Toy – Red
HIGH
CPSC

AiTuiTui Pull String Teething Toys Recalled for Choking Hazard

AiTuiTui recalled its Pull String Teething Toys on January 29, 2026, due to a choking risk. The toys do not meet mandatory safety standards, posing a potential risk of serious injury or death. Consumers should stop using the teething toys immediately and contact the manufacturer for a refund.

AiTuiTui Pull String Teething Toys
The hair
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Recalled Sunneday Oasis Cottage Above-Ground Pool Models 70018 and 70024
MEDIUM
CPSC

Hobby Lobby Recalls Above-Ground Pools Due to Drowning Hazard

Hobby Lobby recalled above-ground pools manufactured by Starmatrix Group on January 29, 2026. The pools pose a drowning risk due to a design flaw that creates a foothold for children. Consumers should stop using these pools immediately and contact Starmatrix for a free repair kit.

Starmatrix Group Inc., of China
The compression
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Violative LuxJet Submersible LED Lights
HIGH
CPSC

LuxJet LED Lights Recalled Due to Battery Ingestion Risk

LuxJet recalled Submersible LED Lights on January 29, 2026, due to ingestion risks from lithium batteries. The recall affects sets of 10 lights sold with multiple batteries. Consumers must stop using the lights and return them for a refund.

LuxJet Submersible LED Lights
The recalled
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Recalled Mindbodygreen Ultimate Multivitamin+ Dietary Supplement Bottle
HIGH
CPSC

Mindbodygreen Recalls Multivitamin Due to Child Poisoning Risk

Mindbodygreen recalled Ultimate Multivitamin+ dietary supplements on January 29, 2026, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating safety standards. Consumers should stop using the product immediately and secure it out of children's reach.

Arizona Nutritional Supplements, of Chandler, Arizona
The bottles
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NorthStar Gas Wet Steam and Hot Water Pressure Washer (Item #157310)
HIGH
CPSC

Northern Tool Recalls Hot Water Pressure Washers Over Fire Risk

Northern Tool + Equipment recalled three models of hot water pressure washers on January 29, 2026. Abnormal burner operation can produce smoke and flames, posing a fire hazard. Consumers should stop using the products immediately and seek repairs.

Northern Tool + Equipment Manufacturing, of Faribault, Minnesota
The fan
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Recalled Sefudun 5% Minoxidil Hair Growth Serum Kit for Men
HIGH
CPSC

Sefudun Hair Growth Serum Recalled Due to Child Poisoning Risk

Nengmiaokeji recalled Sefudun 5% Minoxidil Hair Growth Serum Kit on January 29, 2026. The product lacks child-resistant packaging, posing a serious poisoning risk to children. Consumers should stop using the serum immediately and contact the company for a replacement.

Sefudun
The hair
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Tag Statistics

Total Recalls
2,142

Related Tags

electronicimmediate actionstop use immediatelyreplacement availablefda regulatedexplosion riskelectrical hazardglasssuffocation riskinfant producttoddler productadult product