Food & Beverages
HIGH
FDA FOOD
Black Sheep Egg Company Recalls 46,800 Dozen Free Range Grade AA Eggs Over Salmonella Risk (2025)
Black Sheep Egg Company
Potential Salmonella
garage Recalls
100 recalls tagged with “garage”.
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid Misalignment in 48,110 Units (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Food & Beverages
HIGH
FDA FOOD
Lawrence Wholesale Frozen Shrimp Recalled for Cs-137 Contamination (4,871 Cases, 2025)
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Lawrence Wholesale
Product manufactured
Food & Beverages
HIGH
FDA FOOD
Mars Foods Ben's Original Ready Rice Recalled for Stones in 273 Cases (2025)
Possible presence of stones in product
Mars Foods
Possible presence
Health & Personal Care
HIGH
FDA DEVICE
Argon Medical Devices Recalls 1,821 Option Elite IVC Filters for Dilator Resistance Risk (2025)
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied
Argon Medical Devices
Due to
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound OMNI II TEE Transducer Recall Two Units Nationwide (2025)
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DRUG
Viorele Desogestrel/Ethinyl Estradiol Recall 2025 for Impurities
Viorele
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
ImaCor ClariTEE Miniaturized TEE Probe CLT-010 Recalled Over Reversed Articulation Risk (2025)
Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.
ImaCor
Production assembly
MEDIUM
CPSC
DT Swiss Recalls Carbon Wheels Over Crash Hazard Affecting 2740000 ID Codes and Higher (2025)
DT Swiss
A defect
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens Medical Solutions USA
There is
Food & Beverages
HIGH
FDA FOOD
Middlefield Original Cheese Co-op Recalling 7,455 lbs of Cheese Loaves Over Listeria Contamination (
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative
Potential contamination
Food & Beverages
HIGH
FDA FOOD
Sunrise Creamery Dilly Pickle Monterey Jack Cheese Recalled Over Listeria Risk (2025) by Middlefield
Potential contamination with Listeria monocytogenes
Sunrise Creamery
Potential contamination
Food & Beverages
HIGH
FDA FOOD
Middlefield Original Cheese Cooperative Smoked Cheddar Recalled for Listeria Risk in 2025
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative
Potential contamination
Vehicles & Parts
HIGH
NHTSA
Hyundai Recalls 2025-2026 Santa Fe and Tucson for Engine Fastener Issue
Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Tucson and Santa Fe vehicles. The connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power and engine damage, possibly resulting in an oil leak.
Hyundai
A loss
Vehicles & Parts
HIGH
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled for Safety Architecture Software Issue (41,009 Units, 2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DRUG
B. Braun Sodium Chloride Injection 1000 mL Recalled nationwide for particulates (Class I)
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.
B. Braun Medical Inc.
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Philips CT Systems Brilliance 40/64 Channel and Ingenuity Flex Recalled for Couch Descent Risk (2025
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Philips
The patient
Health & Personal Care
HIGH
FDA DEVICE
Philips CT Systems Recall 2025 Affects 33 Units Worldwide Over Couch Descent Risk
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.
Philips
The patient