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
A lot of Tornier surgical screws is labeled as 5.0mm x 18mm but actually measures 5.0mm x 14mm. If undetected during surgery, the incorrect screw could increase the risk of mechanical failure and require revision surgery.
Olympus is recalling sphincterotomes that did not undergo proper thermoforming, which could cause device deformation and loss of performance. The 5,089 affected units were distributed throughout the US and internationally.
Vivoo Sodium, Vitamin C, and Hydration test strips distributed without FDA clearance may provide inaccurate diagnostic results, potentially leading to inappropriate medical intervention.
The LH One Step Ovulation Test Device was distributed before obtaining required FDA clearance. These test devices may provide false or inaccurate results, potentially leading to inappropriate medical intervention.
Maquet's Venous Bubble Sensor (Model 701055720) is recalled due to connecting cable durability issues that may cause sensor damage or disconnection errors on connected medical devices.
Siemens has recalled NAEOTOM Alpha.Prime CT system software applications that were distributed without FDA 510(k) clearance. Affected systems are located in the US, Canada, Costa Rica, India, and Israel.
Encore Medical recalls EMPOWR Acetabular System hip implant liners due to packaging errors where wrong device components were found in packaging. The discrepancy may cause surgical delay or need for revision surgery.
Nasal jejunal feeding tubes (NJFT-10) from Wilson-Cook Medical are recalled for being packaged without the required nasal transfer tube component, preventing safe use.
ETAC A/S recalls Molift Mover 300 mobile hoists due to bolt deformation in the lifting bar joint that can prevent proper device functionality.
Fujirebio Diagnostics is recalling Lumipulse G pTau 217 Plasma test cartridges due to inaccurate test results that may falsely classify patients as having or requiring additional testing for Alzheimer's disease amyloid pathology.
Menopause test cassette distributed before FDA approval recalled due to risk of false or inaccurate diagnostic results that could lead to inappropriate medical intervention.
Vortex Surgical is recalling Lindsell Sutured IOL Marker scleral markers due to potential voids in sterile pouches. Compromised seals could allow bioburden contamination that may lead to infection.
Maserati is recalling 1,710 Grecale (2023-2024) and GranTurismo (2024) vehicles because software may prevent the backup camera display from functioning. Loss of rear visibility increases collision risk.
Khee Trading, Inc. is recalling frozen half shell oysters potentially contaminated with Norovirus. The product was farm-raised in Korea, imported into the U.S., and distributed across seven states.
Diva Fam Inc is recalling Sea Moss Gel Superfood products due to potential Clostridium botulinum contamination. The affected products were distributed nationwide through 31 retail customers and online sales.
Pending LLM rewrite. Source: NHTSA 25V789000.
Diva Fam Inc is recalling Sea Moss Gel Superfood (16 FL OZ) due to potential Clostridium botulinum contamination. The product was distributed nationwide through retail and online sales.
Rich Products Corp is recalling Gluten Free 14" Seasoned Vegan Pizza Crust due to undeclared milk and egg allergens. Consumers with milk or egg allergies are at risk.
WinCo Foods is recalling Deli Margherita Pizza Thin Crust (Item #67279) distributed across 10 Western states due to potential metal fragments in the product.
General Motors is recalling certain 2024 Chevrolet Silverado and GMC Sierra pickup trucks with power-unlatching tailgates. The tailgate's electronic latch may short circuit due to water intrusion and unlatch while parked, which can result in lost cargo creating a road hazard.
Unichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide tablets for exceeding N-Nitroso Bisoprolol impurity limits. Lot GBHL24005A (expiration 09/2026) was distributed nationwide and in Puerto Rico.
Vortex Surgical Inc. is recalling 25GA Convenience Kits due to potential voids in Tyvek pouch seals that could compromise sterility and lead to infection risk.
Diva Fam Inc is recalling Sea Moss Gel Superfood products due to potential Clostridium botulinum contamination. Products were distributed nationwide through 31 retail customers and online.
Olympus has recalled its Single Use 3-Lumen Sphincterotome V devices due to manufacturing defects. Devices that did not undergo proper thermoforming may deform and lose performance during endoscopic procedures.
Olympus Corporation is recalling Single Use 3-Lumen Sphincterotome V devices due to manufacturing defects. Some devices did not undergo thermoforming and could deform and lose performance.