replacement available Recalls

1,215 recalls tagged with “replacement available”.

Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Tuscan Artichoke and Mozzarella Salad Recalled for Undeclared Allergens (8.5 oz)

Fresh & Ready Foods recalled 233 units of Tuscan Artichoke and Mozzarella Salad distributed to 15 California locations after undeclared wheat and milk allergens were found. The allergen was not declared on the label. Consumers should not eat the product and should contact Fresh & Ready Foods LLC for refunds or replacements via email.

Fresh & Ready Foods
undeclared allergen
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Health & Personal Care
HIGH
FDA DEVICE

Philips Brilliance iCT SP CT Systems Recalled for Descending Couch Hazard in 14 Units Worldwide (202

Philips recalled 14 Brilliance iCT SP CT systems, model 728311, sold worldwide including the United States. The patient support couch may descend unexpectedly to the lowermost position because of ball screw misalignment after a replacement. Hospitals should stop using the device immediately and await manufacturer instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter UniCel DxH 800 Hematology Analyzers Recalled for High Hemoglobin Readings in High-WB

Beckman Coulter recalled the UniCel DxH 800 COULTER Cellular Analysis System configured with the Led HGB photometer. The recall affects models B24802, 629029, and B63322 and related configurations. A design-linked issue can yield erroneously high hemoglobin results when samples have elevated white blood cell counts. Stop using the device and follow the manufacturer’s recall instructions. Contact a

Beckman Coulter
Hematology analyzers
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ingenuity CT System Recall 2025: 285 Units Worldwide

Philips recalled 285 Ingenuity CT systems worldwide, including 728321, 728323 and 728326 models. A ball screw misalignment after a replacement can cause the patient couch to descend to the lowermost position. Hospitals and clinics should stop using the devices and follow Philips recall instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ingenuity CT Brazil 728325 CT System Recalled for 3 Units in 2025

Philips recalled 3 Ingenuity CT Family Brazil systems, Model 728325, distributed worldwide, including the United States. A ball screw misalignment after a replacement may cause the patient support table to descend to the lowest position. Hospitals and clinicians should stop using the device and follow Philips recall instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter DxH 900 COULTER Hematology Analyzer Recalled for Inaccurate Hemoglobin Results

Beckman Coulter recalled hematology analyzers configured with HGB photometers after reports of erroneously high hemoglobin results in samples with elevated WBC counts. The recall covers DxH 900 systems worldwide. Stop using the device immediately and follow manufacturer instructions. Contact Beckman Coulter or a healthcare provider for guidance.

Beckman Coulter
Hematology analyzers
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter UniCel DxH 600 Hematology Analyzer with HGB Photometer Recalled in 2025

Beckman Coulter recalled the UniCel DxH 600 COULTER Hematology Analyzer configured with an LED HGB Photometer, distributed to laboratories worldwide. The device may produce erroneously high hemoglobin results when WBC counts are elevated. Labs and healthcare providers should stop using the device immediately and follow Beckman Coulter's recall instructions.

Beckman Coulter
Hematology analyzers
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Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care Bathing Spa Devices Recall for Missing Unique Device Identifier (Z-1500-2026)

Penner Patient Care recalled 643 devices nationwide after the FDA flagged missing unique device identifiers. The recall affects a broad range of Penner Pacific Bathing Spa models. The device lacks a unique device identifier, posing regulatory and traceability concerns. Stop using the device and follow recall instructions from Penner Patient Care or a healthcare provider.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care Penner Pacific Bathing Spa Recalled for Missing UDI (158 Units)

Penner Patient Care recalled 158 Penner Pacific Bathing Spa devices distributed nationwide in the United States. The device does not bear a unique device identifier. Healthcare providers and patients should stop using the device immediately and follow the recall instructions mailed to affected parties.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care Recalls 26 Penner Pacific Bathing Spa Units for Missing UDI Label (2026)

Penner Patient Care recalled 26 Penner Pacific Bathing Spa units distributed nationwide in the United States after finding they do not bear a unique device identifier. The absence of a UDI prevents reliable traceability of the devices. Healthcare providers and patients should stop using the devices and follow the manufacturer’s recall instructions.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care's Penner Pacific Bathing Spa Recalled for Missing UDI in 21 Units (2025)

Penner Patient Care, Inc. recalled 21 Penner Pacific Bathing Spa units distributed nationwide in the United States after discovering the devices do not bear a unique device identifier. The missing UDI hinders traceability for adverse events and recalls. Consumers should stop using the devices and contact Penner Patient Care for instructions.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Penner Pacific Bathing Spa Recall: 10 Units Missing UDI (2025)

Penner Patient Care recalled 10 Penner Pacific Bathing Spa units nationwide on 2025-08-13 after regulators flagged the device lacks a unique device identifier. The device does not bear a unique device identifier. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Penner Patient Care Bathing Spa Recalled for Missing UDI in 2025

Penner Patient Care recalled 45 Penner Pacific Bathing Spa units distributed nationwide in the United States. The devices do not bear a unique device identifier. Patients and healthcare providers should stop using this device immediately and follow the recall instructions provided by the manufacturer.

Penner Patient Care
The device
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Health & Personal Care
HIGH
FDA DEVICE

Max Mobility/Permobil Recalls 25,389 MX2+ SpeedControl Dial Units (2025)

Max Mobility LLC and Permobil recalled 25,389 MX2-3DC SpeedControl Dial units used with the SmartDrive MX2+ wheelchair power assist. A faulty electrical connection between the speed control dial and the wheelchair motor can cause loss of control. Users should stop using the device immediately and follow the manufacturer’s recall instructions for next steps.

Max Mobility
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Artis Pheno Fluoroscopic X-Ray System Recalled for 20 Units in 2025

Siemens Medical Solutions USA is recalling 20 Artis Pheno image- intensifiied fluoroscopic X-ray systems distributed nationwide. The recall cites limited system movements after startup. Hospitals and healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.

Siemens Medical Solutions USA
Limited system
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Health & Personal Care
HIGH
FDA DEVICE

Max Mobility Permobil MX2+ SpeedControl Dial Recalled for 15,834 Units in 2025

Max Mobility LLC recalls Permobil Smart Drive MX2+ SpeedControl Dial MX2-3DCK affecting 15,834 units sold through multiple retailers. A faulty electrical connection between the speed control dial and the wheelchair motor can cause loss of control. Stop using the device immediately and follow recall instructions; contact Max Mobility LLC or your healthcare provider for instructions. This recall was

Max Mobility
Due to
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Tag Statistics

Total Recalls
1,215

Related Tags

kitchenimmediate actionstop use immediatelyreturn for refundfda regulatedcpsc regulatedburn riskchoking hazardpoisoning risklaceration risksuffocation riskexplosion risk