Safety Recalls

15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 3,551–3,600 of 15,186

• Medical Device Recall · October 31, 2025

  Philips North America Llc

  IntelliVue MP40. Product Number: M8003A.

  Potential issue where the IntelliVue monitors did not alarm.

  Class II

• Medical Device Recall · October 31, 2025

  Philips North America Llc

  IntelliVue Multi Measurement Server X2. Product Number: M3002A.

  Potential issue where the IntelliVue monitors did not alarm.

  Class II

• Medical Device Recall · October 31, 2025

  Philips North America Llc

  IntelliVue MP5. Product Number: M8105A.

  Potential issue where the IntelliVue monitors did not alarm.

  Class II

• Medical Device Recall · October 31, 2025

  Philips North America Llc

  IntelliVue MP20. Product Number: M8001A.

  Potential issue where the IntelliVue monitors did not alarm.

  Class II

• Medical Device Recall · October 31, 2025

  Stryker Medical Division of Stryker Corporation

  Stryker Arise 1000EX mattress, Part Number 2236000000

  Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.

  Class II

• Food Recall · October 30, 2025

  Blue Oven Bakery, Inc.

  Blue Oven Artisan Bakery English Muffins, Net Wt. 13.4 oz (380g), packaged as a 4-pack in a clear plastic bag, UPC 198715684322

  Undeclared allergen - milk

  Class II

• Food Recall · October 30, 2025

  Lotus Vaping Technologies, LLC

  Monarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC

  Product has the potential to be contaminated with Salmonella

  Class I

• Food Recall · October 30, 2025

  Lotus Vaping Technologies, LLC

  Monarch Premium Kratom White Elephant powder is packaged in seal mylar pouches: Monarch Premium Kratom, White Elephant, 4oz powder (112g), UPC 851006008480 Monarch Premium Kratom, White Elephant, 0.

  Product has the potential to be contaminated with Salmonella

  Class I

• Consumer Product Recall · October 30, 2025

  Knog Pty Ltd, of Grapevine, Texas

  Knog Blinder 900 and Blinder 1300 Front Bicycle Lights

  The lithium-ion battery in the bicycle light can overheat and catch fire, posing a risk of fire and burn hazards.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Xuzhou Mingquanhe Household Co., Ltd., of China

  YaFiti Fabric 12-Drawer Dressers

  The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injuries or death to children. The dressers violate the mandatory standard required by the STURDY Act.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Jiangsu Zhi Pai Furniture Manufacturing Co., Ltd., of China

  WLIVE Fabric 16-Drawer Dressers

  The recalled dressers are unstable if they are not anchored to the 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

• Food Recall · October 30, 2025

  Lotus Vaping Technologies, LLC

  Monarch Premium Kratom Bali Gold powder is packaged in seal mylar pouches: Monarch Premium Kratom Bali Gold, 4oz powder (112g), UPC 851006008428 Monarch Premium Kratom Bali Gold, 8oz powder (224g), U

  Product has the potential to be contaminated with Salmonella

  Class I

• Food Recall · October 30, 2025

  Lotus Vaping Technologies, LLC

  Monarch Premium Kratom Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.

  Product has the potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · October 30, 2025

  Inpeco S.A.

  FlexLab (FLX); Version: FLX-217-10;

  The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results. This error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes.

  Class II

• Consumer Product Recall · October 30, 2025

  Huizhou Dingbang E-Commerce Co., Ltd. dba DINBooonLUX, of China

  DINBooonLUX 12-Inch Full Size Hybrid Mattresses

  The mattresses violate the mandatory flammability standard, posing a risk of serious injury or death from fire.

  Unclassified

• Medical Device Recall · October 30, 2025

  Olympus Corporation of the Americas

  Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Number: HX-400U-30 Used with an Olympus endoscope to deliver a nylon loop snare.

  Potential that the ligation loop was unable to release or detach as expected during use, causing the loop to become unintentionally fixed around patient anatomy.

  Class I

• Medical Device Recall · October 30, 2025

  Cepheid

  Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10

  Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.

  Class II

• Consumer Product Recall · October 30, 2025

  shanghaiyizhenwenhuayishuyouxiangongsi dba Harppa, of China

  Harppa 5-in-1 Convertible High Chairs for Babies and Toddlers

  The high chairs pose a risk of serious injury or death to children because they violate the mandatory standard for high chairs. The high chairs were sold without the required attached restraint system, posing a serious risk of falls to children. In addition, a child's head can become trapped in the opening created between the seat and the tray, posing a deadly entrapment hazard.

  Unclassified

• Medical Device Recall · October 30, 2025

  Cepheid

  Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10

  Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.

  Class II

• Consumer Product Recall · October 30, 2025

  PT Champion Mattress Indonesia Manufacturing, of Indonesia

  Avenco and Novilla Mattresses

  The mattresses violate mandatory flammability standards for mattresses, posing a risk of serious injury or death from fire.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Grundens, of Poulsbo, Washington

  Grundens Youth Clipper 282 and Zenith 282 Jacket

  A drawstring in the hood of the recalled jackets presents a substantial product hazard as it can get caught on objects and cause death or serious injury to children, due to strangulation.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Shenzhen Speeding Culture Communication Co. Ltd., dba HOMEAL, of China

  Children's HOMEAL Bed Rails

  The recalled bed rails violate the mandatory standard for children's portable bed rails because when installed adjacent to the bed, a child can become entrapped in the openings on the side of the mattress, posing a risk of serious injury or death due to entrapment.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Euromarket Designs, Inc., dba Crate & Barrel, of Northbrook, Illinois

  Ana Dining Chair

  The legs of the dining chair can break, posing a fall hazard.

  Unclassified

• Consumer Product Recall · October 30, 2025

  H-E-B, LP, of San Antonio, Texas

  Destination Holiday Glow Light Stick Bracelets

  The green glow stick bracelet within the 12-pack container can leak, posing a skin irritation hazard.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Milwaukee Electric Tool Corp., of Brookfield, Wisconsin

  Milwaukee Tool M18 FUELTM Top Handle Chainsaw with either a 12" or 14" bar

  The recalled chainsaw's chain brake may not activate, posing a laceration hazard.

  Unclassified

• Consumer Product Recall · October 30, 2025

  ABL Group, Inc. dba Upperluxe and Modera Store, of Brick, New Jersey

  Organic Cotton Pack N Play Mattress Dual-Sided Portable Baby Crib Pad

  The after-market play yard mattresses may not adequately fit certain play yards, which is in violation of the mandatory standard for crib mattresses, posing a deadly entrapment hazard. Babies have suffocated in gaps between an undersized mattress, or extra padding, and side walls of a product, especially when the infant's face becomes trapped against the side and the mattress, preventing the infant from breathing.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Polaris Industries Inc., of Medina, Minnesota

  Model Year 2025-2026 Ranger XP 1000 NorthStar and Ranger Crew XP 1000 NorthStar Recreational Off-Road Vehicles (ROVs)

  An improperly routed alternator cable can become damaged and contact the negative battery post, resulting in an electrical short, posing a fire hazard and risk of serious injury.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Carole Accessories, Inc., of Los Angeles, California

  Halloween-themed Skeleton Wax Candle

  The candle contains ornaments that are flammable, posing fire and burn hazards.

  Unclassified

• Consumer Product Recall · October 30, 2025

  Werner Paddles, of Tennessee

  Stealth and Covert Kayak Paddles

  The recalled kayak paddles can break during use, posing a drowning hazard.

  Unclassified

• Medical Device Recall · October 30, 2025

  Inpeco S.A.

  FlexLab (FLX); Version: FLX-217-40;

  The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes

  Class II

• Food Recall · October 29, 2025

  Triple B Corporation

  COKE FARM Beans, Green 25 lb. Product of USA Coke Farm San Juan Bautista, CA 95045

  Potential chemical contamination.

  Class III

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  Outlook set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the followin

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the fo

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as th

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  Outlook set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the followin

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Medical Device Recall · October 29, 2025

  B Braun Medical Inc

  Anesthesia IV Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the fo

  Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

  Class II

• Food Recall · October 29, 2025

  Siluetaya, LLC

  SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027

  Product contains yellow oleander

  Class I