All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Recalled Polaris Model Year 2025 Ranger XP 1000 NorthStar
HIGH
CPSC

Polaris Recalls 2025-2026 Ranger XP 1000 NorthStar UTVs for Fire Hazard

Polaris Industries recalled certain VINs of 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar UTVs sold through Polaris dealers nationwide for between $28,000 and $38,000. An improperly routed alternator cable can contact the negative battery post, creating an electrical short and a fire risk. Owners should immediately stop using the recalled vehicles and contact Polaris for a免费

Polaris Industries
An improperly
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Recalled Harppa 5-in-1 Convertible High Chair
HIGH
CPSC

Harppa 5-in-1 Convertible High Chair Recall Expands Over Risk of Fall and Entrapment Hazards (2025)

Harppa recalled 5-in-1 convertible high chairs due to risk of serious injury or death from fall and entrapment hazards. The recall involves model BHC001 with production batch 202408. The chairs were sold in green, pink and gray. Consumers should stop using the product immediately and seek a replacement. Harppa provides a replacement option and destruction instructions for the recalled unit.

Harppa
The high
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Recalled Grundens Youth Zenith 282 Jacket (navy)
HIGH
CPSC

Grundens Recalls Youth Clipper 282 and Zenith 282 Jackets Over Drawstrings Strangulation Hazard (202

Grundens has issued an active recall for the Youth Clipper 282 Jacket and the Youth Zenith 282 Jacket in youth sizes 8 through 12. The jackets have hood drawstrings that can catch on objects, creating a risk of strangulation. Consumers should stop using the jackets immediately and contact Grundens for a full refund or a 20% store credit after removing the drawstrings.

Grundens
A drawstring
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Recalled YaFiti 12-Drawer Rustic Brown Dresser (front view)
HIGH
CPSC

YaFiti Fabric 12-Drawer Dressers Recalled for Tip-Over Hazard on Amazon

YaFiti Fabric 12-Drawer Dressers sold on Amazon are recalled after tip-over and entrapment hazards could cause serious injury. The unanchored dressers can topple when pulled or bumped, posing a risk to children. Consumers should stop using the recalled dressers immediately and contact YaFiti for a full refund.

YaFiti
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Olympus HX-400U-30 Recall: 7,803 Endoscopic Ligation Devices Recalled in 2025

Olympus Corporation of the Americas recalled 7,803 HX-400U-30 single‑use ligating devices distributed nationwide in the United States. The ligation loop may fail to release or detach. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus or their healthcare providers.

Olympus
Potential that
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Health & Personal Care
HIGH
FDA DEVICE

Medicrea Recalls Implant Inserter Over Rotation Failure Risk

Medicrea recalled 44 units of its IB3D Universal Implant Inserter on October 29, 2025. The device's handle may untread from the shaft, preventing proper rotation of implants. The recall affects states including TN, CA, and TX.

Medicrea
Due to
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Blood Administration Set Recall 33,528 Units for Backflow Risk (2025)

B. Braun Medical recalled 33,528 Blood Administration Set units used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The sets have a backflow risk from secondary piggyback IV containers into primary IV containers and may fail to prime. Health-care facilities should stop using the device immediately and follow the recall letter instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Rate Flow IV Set Recalled for 150,664 Units in 2025

B. Braun Medical recalled 150,664 Rate Flow IV Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The devices are cataloged as 375258. The recall addresses a potential backflow from piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s rec

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Vista IV Set Recall for 74,652 Units Over Backflow and Occlusion Risk

B Braun Medical Inc recalls 74,652 Vista IV sets used with Infusomat Space and Vista Basic Pumps due to backflow and occlusion risks. The recall affects devices distributed worldwide, including the US, Canada, Germany, Guatemala, and Singapore. Stop using the device immediately and follow manufacturer instructions.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Outlook IV Set Recall 162,648 Units for Backflow Risk (2025)

B Braun Medical recalled 162,648 Outlook IV Sets used with Infusomat Space Large Volume Pumps and related systems. The devices carry a backflow risk from secondary piggyback IV containers into primary IV containers and may fail to prime. Hospitals and patients should stop using the device immediately and follow recall instructions.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical SAFELINE IV Sets Recalled for 46,250 Units Over Backflow Risk (2025)

B. Braun Medical recalled 46,250 SAFELINE IV sets sold worldwide on Oct. 29, 2025. The devices pose a backflow risk from secondary piggyback IV containers into primary lines and may fail to prime due to occlusion. Hospitals and patients using Infusomat Space Large Volume Pump, Outlook Pump, or Vista Basic Pump with SAFELINE sets should stop use immediately and await manufacturer instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 11,832 Units Over Backflow Risk (2025)

B Braun Medical recalled 11,832 IV administration sets worldwide on Oct 29, 2025. The devices are used with Infusomat Space, Outlook, and Vista Basic Pumps. The hazard is backflow of medication and occlusion. Stop using the product immediately and follow manufacturer recall instructions. Check your model numbers and contact the manufacturer for refunds or replacements.

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall for 187,464 Units Over Backflow Risk (2025)

B. Braun Medical recalled 187,464 IV administration sets worldwide, including US distribution and shipments to Canada, Germany, Guatemala, and Singapore. The devices pose a backflow risk from secondary (piggyback) IV containers into primary containers and can fail to prime properly. Healthcare providers and patients should stop using the devices immediately and follow recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Medicrea Recalls IB3D PL Instruments Set Over Safety Hazard

Medicrea recalled 44 units of its IB3D PL Instruments Set on October 29, 2025. The orthopedic rotation tool handle may untread from the shaft, causing it to fail during use. Healthcare providers and patients must stop using the device immediately.

Medicrea
Due to
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Infusomat IV Sets Recalled for Backflow and Occlusion Risk (49,330,370 Units)

B. Braun Medical recalled 49,330,370 Infusomat IV sets worldwide after a potential backflow from secondary to primary IV containers and an inability to prime. The recall covers gravity IV sets and pump sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Stop using any affected sets immediately and contact B. Braun Medical for instructions on refunds or replacement

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 12,320 IV Burette Sets Over Backflow Risk (2025)

B. Braun Medical Inc. is recalling 12,320 burette sets worldwide used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The device can allow backflow from secondary IV containers into primary containers and may fail to prime. Hospitals and clinics should stop using the device immediately and follow the recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Philips CT Scanner Recalled Over Potential Detachment Hazard

Philips North America recalled six units of the Incisive CT scanner on October 29, 2025, due to a serious safety hazard. The screws on the tube heat exchanger may not be properly tightened, leading to potential detachment during operation. This defect could cause damage to other components within the system.

Philips North America
If the
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (2025)

B Braun Medical Inc recalled 1,019 IV administration sets worldwide after reports of backflow and occlusion. The devices were used with BBMI Infusomat Space, Outlook, and Vista Basic pumps. The recall affects a single catalog number 457506 with UDI details. Patients should stop using the device and follow manufacturer instructions for return.

BBraun Medical
Potential for
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