Severity 1 of 5
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Severity 1 (Low) recalls are typically cosmetic defects, documentation issues, packaging-only problems, and Class III administrative corrections. The product itself is unlikely to cause adverse health consequences. The manufacturer is correcting the issue to comply with FDA or USDA rules, not because anyone is at risk. You can almost always continue using a Severity-1 product without concern.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Philips Ultrasound recalls 171,322 L17-5 Transducer Probes to provide clarification on their useful life. This Class III recall affects devices distributed nationwide.
Philips is recalling 171,322 X3-1 Transducer Probe units nationwide to provide clarified labeling defining the ultrasound transducers' useful life.
Philips Ultrasound is clarifying labeling on the SCNHD LA L7-4 HDI Transducer Probe to better define useful life. The clarification affects approximately 171,322 units distributed nationwide.
Philips Ultrasound recalls 171,322 C9-2 Transducer Probe units to provide clarification and labeling defining the useful life of these medical ultrasound transducers. No illnesses or injuries have been reported.
Philips Ultrasound recalls 171,322 S7-3t transducer probes nationwide to provide labeling clarification regarding the useful life of ultrasound transducers.
Philips Ultrasound, Inc. is recalling 171,322 C9-4v Transducer Probes nationwide. The recall provides labeling clarification regarding the useful life of these diagnostic ultrasound probes.
Philips Ultrasound, Inc. is recalling 171,322 L12-3 Transducer Probes nationwide to provide clarification and labeling regarding the useful life of ultrasound transducers in field use.
Philips Ultrasound is recalling 171,322 units of the C9-3io Transducer Probe to provide clarification and labeling regarding the useful life of the devices. Units were distributed nationwide in the United States.
Philips is recalling approximately 171,322 S7-2t Transducer Probe units to provide labeling clarification and define the product's useful life.
Haleon US Holdings is recalling Sensodyne PRONAMEL Fresh Mint toothpaste due to a labeling error where the tube label states 'Cool Mint/Whitening' instead of 'Fresh Mint.' The actual toothpaste inside is Fresh Mint, as indicated on the carton.
Stickney Hill Dairy recalls Boar's Head Chevre Goat Cheese Cranberry Cinnamon due to an incorrect Use By date printed on the package. The recall affects 372 cases distributed in New York.
AVID Medical recalled the LAP CHOLE PACK surgical kit after the CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized, causing discoloration of the device.
LION Lemon Lime Spring Water Hydration Drink is being recalled due to potential contamination with floating objects. The recall affects 58 cases distributed to three retailers in Tennessee.
D.F.S. International is recalling Daniele brand Extra Virgin Olive Oil because the product may contain Canola Oil instead of Extra Virgin Olive Oil as labeled. Consumers should not consume the product.
Defibtech semi-automated external defibrillators distributed to Switzerland lack required Italian translations of product information and instructions for use, violating Swiss Medical Devices Ordinance requirements for multilingual labeling.
San Miguel Nuts Corp. is recalling Mi More Coco Bandera snacks because the product label fails to declare a color ingredient. The recall affects 3,026 bars distributed to New Jersey.
Akron Pharma is recalling Acetaminophen Regular Strength 325 mg tablets due to incorrect imprinting on the tablets. The recall involves approximately 6,429 bottles distributed nationwide.
Akron Pharma is recalling 324 bottles of Diphenhydramine HCl 50 mg capsules (lot KDC0224001B) due to incorrect identification imprinting on the capsules. The product was distributed nationwide in the United States.
Akron Pharma recalls 456 bottles of Diphenhydramine HCl 25 mg capsules due to incorrect ID imprinted on the capsules.
Remote Diagnostic Technologies Ltd. is recalling Tempus LS-Manual Defibrillator Model 00-3020 units distributed in eight U.S. states. The devices were labeled incorrectly during servicing with wrong product name and CAT number.
Dr. Reddy's Laboratories is recalling ibuprofen 600 mg tablets for failed tablet specifications. The affected product was distributed nationwide.
My Chai Inc is recalling MySyrup Sugar Free Caramel Syrup (604 jugs, nationwide distribution) due to missing production records that prevent verification of proper processing.
My Chai Inc is recalling MySyrup Sugar Free Salted Caramel Syrup nationwide due to lack of production records documenting acidification procedures.
My Chai Inc is recalling 297 jugs of MySyrup Sugar Free Coconut Syrup nationwide due to missing production records. Consumers should not use the product.
Denison Pharmaceuticals recalls Maximum Strength Cough and Chest Congestion and Nighttime Severe Cold and Flu Combo Pack due to crystallization and texture changes in affected bottles.