Safety Recalls
RSS ↗17,560 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,101–5,150 of 17,560
- Class II
Medical Device Recall · October 31, 2025
Olympus OER-ProInform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX450. Product Number: 866062.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX400. Product Number: 866060.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
Olympus OER-MiniInform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct repairs and maintenance.
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
3% Polocaine DENTAL, Mepivacaine Hydrochloride 3% (30mg/mL) (Mepivacaine HCI Injection, USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for DentsplyDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX700. Product Number: 865241.Potential issue where the IntelliVue monitors did not alarm.
- Unclassified
Vehicle Recall · October 31, 2025
2025 KIA TELLURIDEAnti-lock braking or traction control systems that do not function properly can increase the risk of a crash.
- Class II
Drug Recall · October 31, 2025
Phytonadione Injectable Emulsion, USP 10mg/mL, 10x1 mL Single-Dose Vial/carton, Rx Only, Mfd. by: Cipla Ltd. India At M/s Immacule Lifesciences PVT. Ltd. India. Mfd. for: Cipla USA, Inc. Warren, NJ 07Failed Stability Specifications: Observed OOS results: eg results for colour index
- Class II
Drug Recall · October 31, 2025
WeCare, Zinc Oxide Ointment, Net Wt. 15 oz/425 g, Manuactured for: Dynarex Corporation, 11 Dynarex Drive, Middletown, NY 10941, Made in India, NDC 67777-223-05.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP90. Product Number: M8010A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP70. Product Number: M8007A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX600. Product Number: 865242.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX850. Product Number: 866470.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Food Recall · October 31, 2025
First & Last Tavern Traditional Pasta Sauce (meat flavored) 26 FL OZ (1 lb., 10 oz) 737gMay be contaminated with Clostridium botulinum
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
2% Xylocaine DENTAL with Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose cartridges, 1.7 mL each, Rx only, Manufactured for DentsplyDefective container: cracked/broken cartridges
- Class II
Medical Device Recall · October 31, 2025
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
- Class II
Food Recall · October 31, 2025
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lidWheat and Soy missing allergens from the product Contains Statement.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP60. Product Number: M8005A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP30. Product Number: M8002A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP80. Product Number: M8008A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Patient Monitor MX100. Product Number: 867033.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Wecare Enema, 4.5 Fl Oz/133mL, Manufactured for: Dynarex Corporation, 11 Dynarex Corporation, MIddletown, NY 10941 USA, Made in India, NDC 67777-402-01.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP40. Product Number: M8003A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Lanashield Skin Barrier, 4 oz. (113 g), Manfuactured for: Dynarex Corporation, 10 Gleshaw Street, Orangeburg, NY 10962 USA, Made in India, UPC 616784126319.cGMP deviations
- Class I
Food Recall · October 31, 2025
Bulk and Organic Organic Moringa Powder, 44.1lbs bagPossible Salmonella Richmond
- Class II
Medical Device Recall · October 31, 2025
IntelliVue Multi Measurement Server X2. Product Number: M3002A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Nivagen, Zinc Oxide Ointment, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA Made in India, NDC 75834-170-01.cGMP deviations
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP5. Product Number: M8105A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Medical Device Recall · October 31, 2025
IntelliVue MP20. Product Number: M8001A.Potential issue where the IntelliVue monitors did not alarm.
- Class II
Drug Recall · October 31, 2025
Wecare Calasoothe, Net wt. 4 oz (113 g), Manufactured for: Dynarex Corporation, 10 Glenshaw Street, Orangeburg, NY 10962, NDC 67777-234-04.cGMP deviations
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
darby dental supply, MEPIVACAINE, Mepivacaine HCI 3% (30mg/mL) Injection, [Mepivacaine HCI Injection, USP], packaged in a carton containing 50 single-dose Cartridges, 1.7 mL each, Rx only, ManufacturDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Novocol Pharmaceutical of Canada, Inc.
Lidocaine HCI 2% and Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for Patterson DeDefective container: cracked/broken cartridges
- Class II
Drug Recall · October 31, 2025
Dynagel, Moisturizing Wound Hydrogel, Net Wt. 3oz (84.7 g), Manufactured for: Dynarex Corporation, 16 Glenshaw Street, Orangeburg, NY 10962, UPC 61784128016.cGMP deviations
- Class II
Food Recall · October 31, 2025
First & Last Tavern Marinara Sauce (tomato & basil) 26 FL OZ (1 lb, 10 oz) 737gMay be contaminated with Clostridium botulinum
- Class II
Food Recall · October 31, 2025
First & Last Tavern Puttanesca Sauce (olives, capers, hot peppers) 26 FL OZ (1 lb, 10 oz) 737gMay be contaminated with Clostridium botulinum
- 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" barThe recalled chainsaw's chain brake may not activate, posing a laceration hazard.
- Unclassified
Consumer Product Recall · October 30, 2025
Carole Accessories, Inc., of Los Angeles, California
Halloween-themed Skeleton Wax CandleThe candle contains ornaments that are flammable, posing fire and burn hazards.
- Class I
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), UPCProduct has the potential to be contaminated with Salmonella
- Class I
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), UProduct has the potential to be contaminated with Salmonella
- Unclassified
Vehicle Recall · October 30, 2025
2023 JEEP GRAND CHEROKEE, 2023 JEEP WRANGLER, 2024 JEEP GRAND CHEROKEE, 2025 JEEP GRAND CHEROKEEA vehicle fire can increase the risk of injury.
- Class II
Medical Device Recall · October 30, 2025
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.
- Unclassified
Consumer Product Recall · October 30, 2025
shanghaiyizhenwenhuayishuyouxiangongsi dba Harppa, of China
Harppa 5-in-1 Convertible High Chairs for Babies and ToddlersThe 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
Consumer Product Recall · October 30, 2025
PT Champion Mattress Indonesia Manufacturing, of Indonesia
Avenco and Novilla MattressesThe mattresses violate mandatory flammability standards for mattresses, posing a risk of serious injury or death from fire.
- Unclassified
Consumer Product Recall · October 30, 2025
Shenzhen Speeding Culture Communication Co. Ltd., dba HOMEAL, of China
Children's HOMEAL Bed RailsThe 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
ABL Group, Inc. dba Upperluxe and Modera Store, of Brick, New Jersey
Organic Cotton Pack N Play Mattress Dual-Sided Portable Baby Crib PadThe 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.
- Class I
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 II
Medical Device Recall · October 30, 2025
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