Boston Scientific Extractor Pro RX Balloon Catheter Recalled Over Labeling Error (2025)
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
233 recalls tagged with “choking hazard”.
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
Potential contamination with Listeria monocytogenes
Potential contamination with Listeria monocytogenes
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.
Ford Motor Company (Ford) is recalling certain 2025-2026 F-550 SD, F-450 SD, F-350 SD, F-250 SD, and 2025 F-150 vehicles. The Instrument Panel Cluster (IPC) may fail at startup.
One lot manufactured with an invalid sterilization cycle.
Undeclared allergens (sesame and soy).
Mercedes-Benz USA recalls 2025 GLC 350E 4MATIC and related EQE/GLC models due to a loose steering coupling bolt. The defect may loosen the steering rack, risking loss of control. Dealers will tighten bolts at no charge. MBUSA notified owners on Oct 6, 2025.
Product label contains conflicting statements about inclusion and being free of Soy ingredient.
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.

This recall involves three-tiered spiral children's tower toys. The recalled toy has three levels and a basketball hoop with a character's face at the top. The toy measures about 10 inches high by 4 inches wide and came with three yellow balls.
undeclared allergen (Wheat and Milk) on ready to eat sandwiches.
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
The device does not bear a unique device identifier.
Baker’s Authority recalled 70 units of Graham Cracker Meal on August 12, 2025. The product ships to multiple states. Undeclared wheat and soy allergens are listed on the label. The recall urges consumers to avoid consumption and seek refunds or replacements.