repair available Recalls

239 recalls tagged with “repair available”.

Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System Recalled for 602 Reusable Probes (2025)

Olympus Corporation of the Americas recalls 602 ShockPulse-SE Lithotripsy System reusable probes worldwide to hospitals. The recall cites a blinking generator that may fail to recognize the transducer and damage the transducer plug or generator receptacle. Hospitals and patients should stop using SPL-SR probes immediately and follow manufacturer recall instructions.

Olympus
Ongoing investigations
Read more
Recalled Precaliber 20 Bicycle in Miami Green (MY 2024)
MEDIUM
CPSC

Trek and Electra Recall Bicycles With Coaster Brakes Over Crash Hazard (2025)

Trek and Electra recall certain bicycles and replacement rear wheels sold by Trek authorized retailers and Trek.com due to a crash hazard. The coaster brakes can fail to engage, increasing the risk of loss of rider control. Consumers should stop riding recalled bikes, check serial numbers starting with WTU located under the bottom bracket, and contact a Trek or Electra dealer to schedule a free, 3

Trek
The coaster
Read more
Vehicles & Parts
HIGH
NHTSA

Toyota recall affects 2023-2025 models, instrument cluster display may fail

Toyota Motor Engineering & Manufacturing recalls multiple 2023-2025 vehicles because the instrument panel may fail to display speed, braking and tire pressure alerts. Dealers will update software for non-PHEV models and inspect/possibly replace panels for PHEV models at no charge. Owner letters expected Oct 27, 2025. Contact Toyota at 1-800-331-4331; Lexus follow numbers 25LB05/25LA05.

Toyota
An instrument
Read more
Recalled Lezyne Pressure Over Drive Bicycle Tire Pump with analog gauge
MEDIUM
CPSC

Lezyne USA Recalls 2 Bicycle Floor Pumps for Canister Ejection Hazard (2025)

Lezyne USA recalls two bicycle floor pumps, the Pressure Over Drive and Digital Pressure Over Drive, sold at bicycle stores nationwide and online. The canister can eject from the base when pressurized, posing a serious injury risk. Stop using the recalled pumps and contact Lezyne for a free replacement.

Lezyne
The pump's
Read more
Recalled STIHL BR 800 X Magnum Backpack Blower
MEDIUM
CPSC

STIHL BR 800 Magnum Backpack Blowers Recalled for Laceration Hazard (2025)

STIHL is recalling BR 800 Magnum backpack blowers sold through authorized STIHL dealers from May 2025 through September 2025. The recall targets units with serial numbers 546515117 to 547916107. The fan wheel inside the blower can break apart, creating a laceration hazard. Consumers should stop using the recalled units and bring them to an authorized STIHL servicing dealer for a free inspection is

STIHL
The fan
Read more
Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Parasite Test Recalled for Distribution Without Premarket Approval

GET TESTED INTERNATIONAL AB recalled 658 parasite tests distributed nationwide in the United States after regulators flagged distribution without premarket approval. The recall, active as of December 2025, targets devices labeled EAN 7340221707153 and SKU A-PARA. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.

GET TESTED INTERNATIONAL AB
Distribution without
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MP50 Recall 2025 Over Alarm Failure in 1.9 Million Monitors

Philips North America recalled 1,913,441 IntelliVue MP50 patient monitors worldwide after reports the devices did not alarm. The monitors may fail to alert clinicians to patient deterioration. Hospitals should stop using the devices immediately and follow the manufacturer’s recall instructions.

Philips
Potential issue
Read more
Recalled Werner Stealth Kayak Paddle
MEDIUM
CPSC

Werner Paddles Recalls Stealth & Covert Kayak Paddles Over Drowning Hazard (2025)

Werner Paddles recalls Stealth and Covert kayak paddles after determining they can break during use, creating a drowning hazard. The paddles sold by retailers nationwide and online from October 2023 through August 2025 for $470 to $560. Consumers should stop using the recalled paddles immediately and contact Werner Paddles for a full refund or store credit.

Werner Paddles
The recalled
Read more
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
Read more
Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall 122,232 Units Over Backflow Risk (2025)

B. Braun Medical recalled 122,232 IV administration sets sold worldwide through multiple medical distributors. The devices have a backflow risk from secondary (piggyback) IV containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the sets and follow the manufacturer's recall instructions.

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

B. Braun Medical 490238 Extension Set Recalled for IV Backflow Risk (2025)

B. Braun Medical's 490238 Extension Set, used with Infusomat Space Large Volume Pumps and other BBMI devices, is recalled worldwide to hospitals and clinics. The device can allow backflow from secondary piggyback IV containers into the primary container and cannot be primed. Healthcare facilities should stop using the device immediately and follow the manufacturer's recall instructions.

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

BBraun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (490491, 2025)

BBraun Medical Inc recalls 960 IV administration sets distributed worldwide due to backflow risk and inability to prime. The recall affects the IV administration set catalog number 490491 with UDI-DI 04046955086931. The device can allow medication to flow from secondary piggyback containers into primary IV containers and may not prime properly. Stop using immediately and follow recall instructions

BBraun Medical
Potential for
Read more
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
Read more
Recalled Pack-N-Stroll Premium Folding Utility Wagon
HIGH
CPSC

Olympia Tools Recalls Pack-N-Stroll Premium Folding Utility Wagon for 2025 Entrapment and Falls Risk

Olympia Tools International recalls Pack-N-Stroll Premium Folding Utility Wagons sold at Costco after authorities determined the product can trap a child’s head and cause serious injury or death. The defect is an opening between the organizational tray and the sidewall. The wagon also lacks a restraint system. Stop using the wagon now and return it to Costco for a full refund.

Olympia Tools International
The utility
Read more
Recalled Bealife 5-Drawer Dresser (front)
HIGH
CPSC

Bealife 5-Drawer Dressers Recalled for Tip-Over Hazard in 2025

Bealife recalled its 5-Drawer Dressers on Oct. 23, 2025. The dressers are white and measure 32 inches high, 28 inches wide, and 16 inches deep. The model AP23-W is printed on packaging but not on the dresser itself. Consumers should stop using unanchored dressers and seek a full refund.

Bealife
The recalled
Read more