2,756 recalls tagged with “immediate action”.
Philips North America recalls 210 CT systems worldwide after reports that the patient support couch may descend unexpectedly to the lowest position following a replacement. Philips issued a recall dated 2025-08-13 with active status. The recall number is Z-2598-2025. Stop using immediately and follow manufacturer instructions.
HEB recalled 468 cases of 8oz Blueberry Flavored Yogurt Pretzels distributed in Texas by Dollins Pecan Co, Inc. The product contains undeclared wheat allergen. Consumers should not eat the product and should contact Dollins Pecan Co, Inc via email for refund or replacement.
Fresh & Ready Foods recalled 233 units of Chili Crunch Market Mezze sandwiches sold to California private corporate locations. The product contains undeclared wheat, creating a potential severe allergic reaction. Consumers should not consume the product and should contact Fresh & Ready Foods for refund or replacement.
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.
Philips North America LLC recalled 33 CT systems worldwide after reports of a patient couch descending unexpectedly. The affected models are 728242, 728243, and 728244. Hospitals and clinics should stop using the devices immediately and await recall instructions.
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 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 recalled 24 CT systems worldwide after finding that the patient support couch may descend unexpectedly following a replacement. The defect involves a misaligned ball screw in the couch mechanism. Hospitals and imaging centers should stop using the device immediately and follow Philips recall instructions.
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 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 recalled the UniCel DxH 690T COULTER Cellular Analysis System configured with the LED HGB Photometer REF C34520. The hematology analyzer may produce erroneously high hemoglobin results on samples with elevated white blood cell counts. Labs should stop using the device immediately and follow Beckman Coulter's recall instructions.
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 recalled 73 Brilliance CT systems worldwide after determining a ball screw misalignment could cause the patient couch to descend to the lowermost position. The recall covers Brilliance 16 Power, 728240; Brilliance CT 16 Slice, 728246; and Brilliance CT 6 Slice, 728256. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions immediately.
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.
Fresh & Ready Foods recalled 233 Spanish Club Ciabatta sandwiches sold to 15 California locations after discovering undeclared wheat and milk allergens. The recall is Class I and the hazard is an undisclosed allergen on ready-to-eat sandwiches. Consumers should not eat the sandwiches and should contact Fresh & Ready Foods for refunds or replacements by email.
Fresh & Ready Foods recalled 233 Piccolo Pranzo Box sandwiches after undeclared wheat and milk allergens were detected. The product was distributed to 15 California locations. Consumers should not eat the product and should contact Fresh & Ready Foods for refund or replacement information via email.
Penner Patient Care recalls 206 US units of the Penner Pacific Bathing Spa after the device lacks a unique device identifier. The recall targets models listed with multiple variations and serial numbers. Consumers should stop using the device immediately and follow manufacturer instructions.
Penner Patient Care recalled 25 Penner Pacific Bathing Spas nationwide after confirming the device does not bear a unique device identifier. The missing UDI impedes traceability and oversight. Stop using the device and follow the manufacturer’s recall instructions.
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 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.