replacement available Recalls

280 recalls tagged with “replacement 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
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE SPL-S Lithotripsy System Recalled 1,082 Units in 2026

Olympus Corporation of the Americas is recalling 1,082 ShockPulse Lithotripsy System SPL-S single-use probes worldwide. Investigations found the device’s generator may blink and fail to recognize the transducer, risking damage to the transducer plug or generator receptacle. Hospitals and clinics should stop using the device immediately and follow the recall instructions from Olympus.

Olympus Corporation of the Americas
Ongoing investigations
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System SPL-G Recall Impacts 1,684 Units Worldwide (2025)

Olympus Corporation of the Americas is recalling 1,684 ShockPulse-SE Lithotripsy System generators worldwide, including SPL-G models. Investigations found the generator can blink and fail to recognize the transducer, and damage to the transducer plug or generator receptacle may occur. Healthcare providers and patients should stop using the device immediately and follow recall instructions provided

Olympus Corporation of the Americas
Ongoing investigations
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Health & Personal Care
HIGH
FDA DRUG

Nivagen Zinc Oxide Ointment Recall 912 Containers Over cGMP Deviations (2025)

Nivagen Zinc Oxide Ointment 20% skin protectant, manufactured in India for Nivagen Pharmaceuticals and distributed nationwide in the USA, is recalled. The recall covers 912 containers. The defect cited is cGMP deviations. Consumers and healthcare providers should stop using the product and follow guidance from Blossom Pharmaceuticals or a healthcare professional.

Nivagen Zinc Oxide
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

Philips IntelliVue MX700 Recall Affects 1,913,441 Monitors Worldwide (2025)

Philips North America LLC is recalling 1,913,441 IntelliVue MX700 patient monitors (Product Number 865241) distributed worldwide. The monitors may fail to alarm. Hospitals and clinicians should stop using the affected devices immediately and follow the recall instructions.

Philips North America
Potential issue
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Food & Beverages
HIGH
FDA FOOD

Oceans Kitchen Imitation Crabmeat Recalled Over Botulism Risk

Oceans Kitchen recalled 496 cases of imitation crabmeat on September 30, 2025. The product may contain Clostridium botulinum due to temperature abuse during storage. Consumers should not consume the product and seek refunds.

Ocean's Kitchen
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)

Philips Ultrasound recalled 2 units of the Philips OMNI II TEE Ultrasound Transducer sold nationwide through multiple retailers. The recall seeks labeling clarification to define the transducer's useful life. Healthcare facilities should stop using the devices and follow Philips recall instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips X7-2 Ultrasound Transducer Recall for 5 Units Nationwide (2026)

Philips Ultrasound recalled 5 X7-2 ultrasound transducers distributed nationwide to healthcare providers. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare facilities should stop using the recalled devices and follow Philips Ultrasound, Inc instructions or contact their provider for guidance.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound L17-5 Transducer Recalled for Useful-Life Labeling (2025)

Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.

Philips Ultrasound
To provide
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Health & Personal Care
LOW
FDA DEVICE

Philips S4-1 Ultrasound Transducer Recall: 41 Units Nationwide in 2025

Philips Ultrasound, Inc. recalled 41 S4-1 Ultrasound Transducers distributed nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field. Healthcare providers should stop using these devices immediately and follow the recall instructions from Philips or their facility.

Philips Ultrasound
To provide
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Health & Personal Care
LOW
FDA DEVICE

Philips 3D6-2 Ultrasound Transducer Recalled for Labeling Clarification (17 Units, 2025)

Philips recalled 17 units of the 3D6-2 Ultrasound Transducer distributed nationwide to healthcare facilities in the United States. The recall seeks to clarify labeling defining the transducer’s useful life. Clinicians and facilities should stop using the device immediately and follow Philips recall instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound S5-2 Transducer Recall 2025 - 1 Unit Nationwide

Philips Ultrasound recalled 1 unit of the S5-2 Ultrasound Transducer sold nationwide through healthcare distributors. The recall clarifies labeling to define the useful life of the transducer in the field. Healthcare providers should stop using the device and contact Philips Ultrasound for instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound X3-1 Transducer Recalled for Labeling Clarification in 2026 (17 Units)

Philips Ultrasound recalled 17 X3-1 ultrasound transducers nationwide in the United States. The recall is to provide clarification and labeling to define the useful life of transducers in the field. Healthcare providers and patients should stop using the affected devices immediately and await further manufacturer instructions.

Philips Ultrasound
To provide
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)

Philips Ultrasound recalled 1 unit of the C9-4 Ultrasound Transducer, Model No. 989605365021, distributed nationwide in the United States. The recall focuses on clarifying and labeling the device’s useful life. Healthcare providers and patients should stop using the device immediately and follow Philips’ instructions for replacement or further steps.

Philips Ultrasound
To provide
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Food & Beverages
HIGH
FDA FOOD

Herbal Creations Colostrum Powder Recall for Milk Allergen Labeling Error (2025)

Herbal Creations recalls 19,425 kilograms of bulk colostrum powder distributed to 30 US customers after a milk allergen labeling error. The product label does not declare milk as an allergen. Consumers who purchased this product should not consume it and should contact Herbal Creations USA for refund or replacement.

Herbal Creations
Bulk packaged
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Recalled DT Swiss Carbon Fiber Road Wheels
MEDIUM
CPSC

DT Swiss Recalls Carbon Wheels Due to Crash Hazard

DT Swiss recalled carbon fiber road wheels due to a structural defect that may cause crashes. The recall affects wheels with model codes ERC 35mm/45mm, CRC 35mm/45mm, HEC 35mm/45mm, and ARC 50mm/55mm/65mm. Consumers should stop using these wheels immediately and contact the company for a replacement.

DT Swiss
A defect
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter MicroScan Neg MIC 56 Panels Recalled for Contamination Risk (2026)

Beckman Coulter recalled 685 boxes of MicroScan Neg MIC 56 panels distributed nationwide to U.S. healthcare facilities after contamination was reported in wells. Contamination could lead to unreliable antimicrobial susceptibility and organism-identification results. Health care providers should stop using the panels and follow Beckman Coulter recall instructions immediately.

Beckman Coulter
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Summa Therapeutics Recalls 22 Finesse BTK Multicath Angioplasty Balloons Over Burst Specifications (

Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.

Finesse BTK Multicath
Potential for
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Tag Statistics

Total Recalls
280

Related Tags

electrical hazardimmediate actionstop use immediatelyreturn for refundrepair availablefda regulatedelectronicpoisoning riskkitchencpsc regulatedchemical hazardsuffocation risk