Safety Recalls

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17,560 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 5,351–5,400 of 17,560

Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50, iM60, iM70, iM80 Product Description: The iM series Patient Monitor including iM50, iM60, iM70 and iM80 can perform long-t
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8, iM8A, iM8B Product Description: iM8 Series Patient Monitor can perform long-time continuous monitoring of multiple physiolo
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog Number: MFM-CMS Product Description: MFM-CMS is a central monitoring system product, which can connect and manage information
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3A Product Description: The Vital Signs Monitor is a portable device intended for use by health care professionals. The mon
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3 Product Description: The iM3 has three work modes, Monitor, Spot and Round, to measure physiological parameters, includi
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Food Recall · October 24, 2025
E.A. Sween Co.
Deli Express BBQ Pulled Pork on a sesame bun. Net Wt 5.5oz (156g) UPC 0 41433-03087 5. EA Sween Company, Eden Prairie, MN 55344.
Potential foreign material (plastic)
Class II
Medical Device Recall · October 24, 2025
Siemens Medical Solutions USA, Inc
MAMMOMAT Inspiration;
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
Class II
Food Recall · October 24, 2025
Twin Sisters Creamery, LLC
Twin Sisters Creamery Peppercorn cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingredients: cultured raw cow's milk, whole peppercorns, salt, enzymes. Made in Fer
Raw milk Peppercorn cheese is recalled due to E.coli O26:H11
Class I
Medical Device Recall · October 24, 2025
Siemens Medical Solutions USA, Inc
MAMMOMAT Fusion;
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: X8, X10, X12 Product Description: The X8 X10 X12 Patient Monitor (hereinafter called X series) can perform long-time continuous
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Drug Recall · October 24, 2025
Cipla USA, Inc.
Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., (a subsidary of Cipla Ltd) Hauppauge, NY 11786, Manufactur
Failed stability specifications: Out of specification for hardness test
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite V5, elite V6, elite V8 Product Description: V series Patient Monitor including elite V5, elite V6 and elite V8 which can p
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Siemens Medical Solutions USA, Inc
MAMMOMAT Revelation;
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
Class II
Drug Recall · October 24, 2025
Cipla USA, Inc.
Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., Hauppauge, NY 11786, Manufactured for : Cipla USA, Inc., 1
Failed stability specifications: Out of specification for hardness test
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog Number: F6, F9, F6 Express, F9 Express Product Description: The devices are bedside fetal and maternal monitors, which are used
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10, iX12, iX15 Product Description: The iX series Patient Monitors including iX10, iX12, iX15 can perform long-time continuous
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3 Product Description: The Vital Signs Monitor is a portable device intended for use by health care professionals. The moni
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3B Product Description: M3B Vital Signs Monitor is a patient monitoring device providing the patient with a continuous vita
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
GE Medical Systems, LLC
Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography
Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR ¿1020.30(j).
Class II
Food Recall · October 24, 2025
Twin Sisters Creamery, LLC
Twin Sisters Creamery Whatcom Blue cheese, 2.5lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingredients: cultured raw cow's milk, salt, enzymes, penicillium roqueforti. Ma
Raw milk Whatcom Blue cheese is recalled due to E. coli O103:H2.
Class I
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3s, iM3As, iM3Bs, iHM3s Product Description: The iM3s series vital signs monitors including iM3s/iM3As/iM3Bs/iHM3s are int
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2, F3 Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological param
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Vehicle Recall · October 24, 2025
Ford Motor Company
2025 FORD EXPLORER, 2025 LINCOLN AVIATOR
Reduced visibility while driving can increase the risk of a crash.
Unclassified
Food Recall · October 24, 2025
Water Pure, Inc.
My Bladder; Supports normal bladder tone & control; Dietary Supplement; packaged in white HDPE bottle with a white cap; bottle size is 150 CC; the net contents in 60 clear capsules containing brown po
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Class II
Food Recall · October 24, 2025
MeriCal, LLC
Member's Mark Super Greens Dietary Supplement; 48 servings; Net Weight 18.28 oz (518.4g) UPC: 193968490775
Potential contamination of Salmonella Richmond
Class I
Food Recall · October 24, 2025
Twin Sisters Creamery, LLC
Twin Sisters Creamery Farmhouse Cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingredients: cultured raw cow's milk, salt, and enzymes. Made in Ferndale, WA. www.t
Raw milk Farmhouse cheeses are recalled due to E. coli O103:H2 and E. coli O74:H25.
Class I
Food Recall · October 24, 2025
Twin Sisters Creamery, LLC
Twin Sisters Creamery Mustard Seed cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingredients: Cultured raw cow's milk, salt, whole yellow mustard seeds and enzyme
Raw milk Mustard Seed cheese is recalled due to E. coli O103:H2 and E. coli O74:H25.
Class I
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog Number: MFM-CNS, MFM-CNS Lite Product Description: The MFM-CNS and MFM-CNS Lite are clinical data managing software applicatio
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Medical Device Recall · October 24, 2025
Edan Diagnostics
Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number: iT20 Product Description: iT20 collects physiological parameters by ECG cables and SpO2 sensors, then achieves data analyz
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class II
Consumer Product Recall · October 23, 2025
Cranach Hardware, of China
Cranach Hardware Plastic Tip Restraint Kits
The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in serious injuries or death to children or elderly consumers interacting with furniture that is secured to the wall with the defective plastic tip restraints.
Unclassified
Vehicle Recall · October 23, 2025
Maserati North America, Inc.
2023 MASERATI GRECALE
Improperly aimed headlights can result in insufficient illumination of the road, reducing the driver's visibility, and increasing the risk of a crash.
Unclassified
Drug Recall · October 23, 2025
Zydus Pharmaceuticals (USA) Inc
Bromocriptine Mesylate Capsules, USP, 5 mg, 30 Capsules per bottle, Rx Only. Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals, Pennington, NJ 08534. ND
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.
Class II
Consumer Product Recall · October 23, 2025
Olympia Tools International, Inc. of Covina, California
Pack-N-Stroll Premium Folding Utility Wagon
The utility wagon violates the mandatory standard for strollers because an opening between the organizational tray and the sidewall may cause a child's head to become entrapped, posing a risk of serious injury or death. In addition, the utility wagon's lack of a restraint system poses a risk of falls to children.
Unclassified
Consumer Product Recall · October 23, 2025
Scepter, of Canada
Scepter Gas and Oil Combination Fuel Containers
The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly risk of flash fire. In addition, the Children's Gasoline Burn Prevention Act requires all closures on portable gasoline fuel containers to be child resistant. The spout on the products is not child-resistant, posing a risk of burn and poisoning to children.
Unclassified
Medical Device Recall · October 23, 2025
Becton Dickinson & Co.
BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
Class II
Food Recall · October 23, 2025
Ice Cream Factory, LLC
Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12 Strawberry Cheesecake with graham cracker swirl, 2.5-gal Tub, Net Weight 14 pounds Labels
Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products
Class II
Medical Device Recall · October 23, 2025
Datascope Corp.
Cardiosave Rescue
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
Class III
Consumer Product Recall · October 23, 2025
3M Company, of St. Paul, Minnesota
Scotch™ brand TL909-50 thermal laminator
The recalled thermal laminators may overheat, posing a burn hazard to consumers.
Unclassified
Vehicle Recall · October 23, 2025
Honda (American Honda Motor Co.)
2025 HONDA CB1000SP
The inability to shift gears while riding increases the risk of a crash or injury.
Unclassified
Consumer Product Recall · October 23, 2025
J & D Brush Co., LLC of Commack, New York
Bio Ionic One-Inch-Long Barrel Curling Iron
The barrel of the curling iron can snap and detach, posing a burn hazard to consumers.
Unclassified
Consumer Product Recall · October 23, 2025
Pro Recycle of Montreal, Quebec, Canada
Scepter Gas and Oil Combination Fuel Containers
The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act, posing a deadly risk of flash fire. In addition, the Children's Gasoline Burn Prevention Act requires all closures on portable gasoline fuel containers to be child resistant. The spout on the product is not child-resistant, posing a risk of burn and poisoning to children.
Unclassified
Vehicle Recall · October 23, 2025
Ford Motor Company
2023 FORD BRONCO
A seat with a dislodged bolt may not properly restrain an occupant in a crash, increasing the risk of injury.
Unclassified
Medical Device Recall · October 23, 2025
Datascope Corp.
Cardiosave Hybrid
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
Class III
Food Recall · October 23, 2025
Echo Lake Foods, Inc.
EchoLakeFoods MF 3067 CNFREE Cage Free Precooked IAF Scrambled Eggs Net Wt. 28 lbs. Bulk. Keep Frozen. Manufactured by: Echo Lake Foods, Inc., 2319 Raymond Ave. Franksville, WI 53126.
Potential Listeria monocytogenes contamination.
Class I
Vehicle Recall · October 23, 2025
Chrysler (FCA US, LLC)
2023 RAM PROMASTER, 2024 RAM PROMASTER, 2025 RAM PROMASTER
Electrical circuits that overheat increase the risk of a fire.
Unclassified
Consumer Product Recall · October 23, 2025
Shenzhen Quanyuanfa Trading Co., Ltd. dba Bealife, of China
Bealife 5-Drawer Dressers
The recalled dressers are unstable if they are not anchored to a wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
Unclassified
Consumer Product Recall · October 23, 2025
Mobility Source Medical Technology Co., Ltd, of China
LEACHOI Bed Rail
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
Unclassified
Consumer Product Recall · October 23, 2025
Lifepro Fitness, of Howell, NJ
Bioremedy Infrared Sauna Blankets
The sauna blankets can overheat, posing a burn hazard.
Unclassified
Consumer Product Recall · October 23, 2025
Sauna360, Inc., of Cokato, Minnesota
Tylö Halmstad and Kiruna Hybrid Saunas
The saunas contain a bench that can collapse, posing a fall hazard to consumers.
Unclassified