Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
Olympus Corporation of the Americas is recalling Olympus Thunderbeat II Shears (Model TB2-0520FC) because the distal tip component may detach during use.
EL MEXICANO horchata drink is recalled for undeclared milk allergen. The voluntary recall affects products in the U.S., Canada, and Japan.
Angiodynamics is recalling specific lots of Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided devices due to a manufacturing defect that may prevent guidewire passage through the catheter hub.
Olympus Corporation of the Americas is recalling OER-ELITE Endoscope Reprocessor Connecting Tubes (Model MAJ-2116) because the Version 2 reprocessor connecting tube lock levers may fail prematurely.
Angiodynamics is recalling Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided devices because a manufacturing defect may prevent guidewires from passing through the catheter hub.
Davol, Inc. is recalling Avitene Ultrafoam Microfibrillar Collagen Hemostat (Catalog Number 1050030) because the product may contain foreign matter, confirmed to be inspect fragments.
Angiodynamics is recalling Soft-Vu Angiographic Catheters (Omni Flush, Non-Braided) due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
Angiodynamics is recalling Soft-Vu Angiographic Catheter, Kumpe, Non-Braided devices due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
Diversatek Healthcare is recalling Viper 3-Stage Wire Guided Balloon Dilators because the catheter inflation tag may contain an incorrect part number with wrong balloon diameter sizes and inflation pressures.
Medline Industries is recalling Convenience Kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects 270,311 units distributed nationwide and internationally.
Marquez Brothers International is recalling Bulk Horchata Powder nationwide due to undeclared milk, a major food allergen. The recall affects approximately 2,494 cases distributed across 29 U.S. states and international locations.
Olympus is recalling Thunderbeat II 5mm ultrasonic surgical shears (model TB2-0535FC) due to potential detachment of the distal tip component during use. Approximately 3,360 units have been distributed internationally.
Summit Import Corporation is recalling Spice Powder due to lead levels exceeding the NYSAGM safety standard. The recalled product was distributed to New York, New Jersey, South Carolina, Maine, Florida, Pennsylvania, Massachusetts, and Virginia.
Angiodynamics recalls Soft-Vu Angiographic Catheters with a manufacturing defect preventing proper guidewire passage through the catheter hub. The affected devices may not function as intended. No injuries have been reported.
Diversatek Healthcare has recalled the Viper 3-Stage Wire Guided Balloon Dilator because the inflation tag may contain incorrect balloon diameter sizes and inflation pressures. The incorrect specifications could affect proper device use during medical procedures.
Olympus is recalling Thunderbeat II ultrasonic surgical shears (Model TB2-0525FC) due to potential detachment of the distal tip component during use.
Mondelez is recalling CHIPS AHOY! Baked Bites Brookie due to hard corn starch lumps found in the product. The recall affects 437 cases distributed to multiple states.
Medline Industries recalled convenience kits containing syringes due to unapproved design changes outside FDA clearance. The recall affects 270,311 units distributed in the US, Canada, Panama, and Barbados.
Arrow International is recalling Pressure Injectable Arrowg+ard Blue Plus central venous catheter kits due to incorrect liquid adhesive manufacturing. Approximately five units were distributed in nine states.
LSL Healthcare is recalling its Foley Urine Collection Kit (Model 1555) because it contains Webcol Large Alcohol Prep Pads that are non-sterile. The kits were distributed nationwide in Maryland, Illinois, and Minnesota.
Arrow International is recalling 115 units of its percutaneous sheath introducer with 7.5–8 Fr catheter because the liquid adhesive was incorrectly manufactured by a supplier. The product is used for venous access and central circulation catheterization.
Olympus is recalling Thunderbeat II Shears (5mm, 45cm) because the distal tip component may detach during use, potentially causing patient harm.
LSL Healthcare is recalling its Wound Closure Tray (Model 7554) distributed nationwide to Maryland, Illinois, and Minnesota because the kits contained non-sterile Webcol Large Alcohol Prep Pads.
Angiodynamics is recalling Soft-Vu Angiographic Catheter Kumpe units due to a manufacturing defect that may prevent guidewires from passing through the catheter hub.
Foundation Medicine is recalling Sequencing Agent SEQ0067, a component of the FoundationOne CDx test, due to a possible increase in phasing that could result in false-positive BARD1 splice site indel artifact variants.