FoodClass II
Power Plate Meals, LLC Recalls Frozen Meatloaf Products Due to Misbranding and Undeclared Allergens
Low - Class II · Class II
· USDA FSIS · MN, ND, SD
Recalls
Safety recalls that rarely make the news, straight from the official U.S. agency records (FDA, USDA, CPSC, NHTSA). Every listing links to its official notice. We only copy what the record says.
Checked Nov 3, 6:52 PM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
1107 recalls
FoodClass III
CAMPO RICO FOODS LLC recalls Kanni Delight 31/40 Fresh Frozen Vannamei White Shrimp IQF
Nitrofurans detected in product
· FDA · LA
Medicines & devicesClass II
Freudenberg Medical, LLC recalls 2 products
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flange contains a Large Esophageal Flange.
· FDA · Nationwide
Medicines & devicesClass I
Boston Scientific Neuromodulation Corporation recalls INFINION CX LEAD KIT
Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which may lead to inadequate stimulation, additional intervention, i
· FDA · NY
Medicines & devicesClass II
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls 3 products
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
· FDA · Nationwide
Medicines & devicesClass II
Windstone Medical Packaging, Inc. recalls 8 products
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier
· FDA · Nationwide
Medicines & devicesClass II
Medtronic Neurosurgery recalls Ventriculostomy Kit
Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospina
· FDA · Nationwide
Medicines & devicesClass II
Paragon 28, Inc. recalls P28 PHANTON INTRAMEDULLARY NAIL SYSTEM
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
· FDA · Nationwide
Medicines & devicesClass II
BD SWITZERLAND SARL recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and
Products may not have received adequate sterilization processing.
· FDA · 26 states
Medicines & devicesClass II
Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
· FDA · Nationwide
Medicines & devicesClass II
Medtronic MiniMed, Inc. recalls MiniMed Go App
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This coul
· FDA · Nationwide
Medicines & devicesClass II
Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit - UHI-4
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
· FDA · Nationwide
Medicines & devicesClass II
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control
· FDA · Nationwide
Medicines & devicesClass II
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control
· FDA · Nationwide
FoodClass I
Western Mixers Produce & Nuts, Inc. recalls FIRST STREET Dark Chocolate Raisins Net Wt
Undeclared peanuts.
· FDA · CA
Medicines & devicesClass II
Intersurgical Inc recalls 2 products
Devices could potentially be occluded or partially occluded.
· FDA · Nationwide
Medicines & devicesClass II
Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
· FDA · Nationwide
Medicines & devicesClass II
TISSIUM SA recalls 8 products
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may resu
· FDA · Nationwide
Medicines & devicesClass II
Argon Medical Devices, Inc recalls 2 products
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lea
· FDA · 28 states
FoodClass II
Vintage Roots LLC recalls Vintage Roots Root Beer Syrup
Unapproved food additive: sassafras bark.
· FDA · MT
FoodKids & BabiesClass I
NARA ORGANICS INC recalls a
Product may be contaminated with Clostridium botulinum.
· FDA · Nationwide
FoodClass I
Adams Extract & Spice LLC recalls 5 products
Undeclared Sesame allergen
· FDA · TX
Medicines & devicesClass II
Boehringer Ingelheim Pharmaceuticals, Inc. recalls Synjardy XR Tablets (empagliflozin and metformin hydrochloride extended-release tablets)
CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been used for a different product.
· FDA · OH
Medicines & devicesClass II
Sarnova HC, Llc recalls Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk)
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls 16 products
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the s
· FDA · Nationwide
Medicines & devicesClass II
Tosoh Bioscience Inc recalls ST AIA-Pack Testosterone
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause falsely elevated or falsely low total testosterone resul
· FDA · Nationwide
FoodClass II
Wondermade LLC recalls Alabama Banana Pudding Marshmallow
Foreign material: small metal pieces
· FDA · FL, IN, PA, TX
Medicines & devicesClass II
BioMed Laboratories, LLC. recalls Medline Remedy Specialized Silicone Cream (Hydraguard-D )
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.
· FDA · Nationwide
Medicines & devicesClass II
CareFusion 213, LLC recalls 10 products
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
· FDA · Nationwide
Medicines & devicesClass II
Oxos Medical Inc recalls Brand Name: OXOS Medical
Due to a defective circuit board that overheats
· FDA · Nationwide
Recall data comes from official U.S. government sources: openFDA (food, drugs, devices), USDA FSIS (meat, poultry, egg products), CPSC (consumer and children’s products) and NHTSA (vehicles, equipment, car seats). openFDA notes its data should not be relied on for medical decisions. Always confirm with the official notice. Check your vehicle by VIN at nhtsa.gov/recalls.