Safety Recalls
RSS ↗15,362 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 8,151–8,200 of 15,362
- Class II
Medical Device Recall · February 6, 2025
LAPAROSCOPY PACK, Model No. CALS41F, CALS41F-01, CALS41GACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Vehicle Recall · February 6, 2025
Mitsubishi Motors North America, Inc.
2023 MITSUBISHI OUTLANDER, 2023 MITSUBISHI OUTLANDER PHEV, 2024 MITSUBISHI OUTLANDER, 2025 MITSUBISHI OUTLANDER PHEVA rearview image that does not display properly reduces the driver's view of what is behind the vehicle, increasing the risk of a crash.
- Class II
Medical Device Recall · February 6, 2025
SPINE LUMBAR PACK , Model No UTSL72AA UTSL72ABACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Vehicle Recall · February 6, 2025
2024 BATTLE MOTORS LET2, 2025 BATTLE MOTORS LET2A loose or detached steering wheel can cause a loss of control, increasing the risk of a crash.
- Class II
Medical Device Recall · February 6, 2025
LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07BACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
EAR PACK , Model No SFEA12AACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Consumer Product Recall · February 6, 2025
Ariens Company, of Brillion, Wisconsin
Ariens® DELUXE-, PLATINUM- and PROFESSIONAL-series Snow ThrowersThe recalled snow thrower impeller and auger assembly can continue rotating even after the operator control lever is released, posing a laceration hazard if a user makes contact with the rotating parts inside the housing enclosure at the front of the machine.
- Class II
Medical Device Recall · February 6, 2025
GENERAL LAPAROSCOPIC PACK-LF , Model No UTGL53S-06 UTGL53S-07 UTGL53S-08ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
C-SECTION PACK, Model Nos LLCS44F LLCS44F-01ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Consumer Product Recall · February 6, 2025
Rainbow Trade (HK) Co. Limited, of Hong Kong
UVIPC Baby GatesThe recalled baby gates violate the federal safety regulations for expansion gates and expandable enclosures. For the versions with a pet door, a child's torso can fit through the secondary opening and, for the other versions that are adjustable, a child's torso can fit through the opening between the gate slat and side wall. These violations pose an entrapment hazard to children.
- Class II
Medical Device Recall · February 6, 2025
C-SECTION PPS , Model No LLCI66M LLCI66M-02 LLCI66M-03 LLCI66M-04ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Consumer Product Recall · February 6, 2025
TravisMathew LLC, of Huntington Beach, California
TravisMathew Women's Sweatshirts and Women's and Men's HoodiesThe recalled sweatshirts and hoodies violate the federal flammability standard for clothing, posing a burn hazard to consumers.
- Class I
Food Recall · February 6, 2025
Jack & The Green Sprouts, Inc.
Jack & the Green Sprouts Alfalfa Sprouts. Net Weight 5 oz. (152g). UPC 7 63247-19891 5. Keep Refrigerated. Product of USA. River Falls, WI 54022.Sprouts have the potential to be contaminated with Listeria monocytogenes
- Class II
Medical Device Recall · February 6, 2025
AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. Manufacturer's Product Numbers (Catalog Number): (1) ASX15/60 and (2) ASX15/80Possibility for the obturator to break (separate).
- Class II
Medical Device Recall · February 6, 2025
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, with Component PCB, TSI/RSI firmware C29278Beckman Coulter identified that an issue for DxI 9000 tip stocker interface (TSI) and reagent storage interface (RSI) boards with the firmware version 1.1.0.0 can cause sub-system communication failures. This failure could result in a delay in reporting patient results.
- Class II
Medical Device Recall · February 6, 2025
BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF: 1116-00, CII Safe ES Desktop PC, REF: 1156-00, CII Safe ES Desktop PC, WiredSync timeout may occur between the server and automated dispensing device, due to a server software error which may occur if syncing a large amount of data that takes excessive time, which may cause the dispensing devices to become disconnected from the ES server; dispensing devices will not receive updated information, which may lead to incorrect therapy, and delay in accessing medication.
- Class II
Medical Device Recall · February 6, 2025
OPEN HEART A PACK , Model No UTOH19AI UTOH19AJ-01 UTOH19AJ-02ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Class II
Medical Device Recall · February 6, 2025
CV BASIC PUMP PACK , Model No WECV23DACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.
- Unclassified
Consumer Product Recall · February 6, 2025
Doosan Bobcat North America, of West Fargo, North Dakota
Bobcat & Steiner AirFX Finish Mower Deck attachmentsThe recalled mower decks cannot be secured in the upright or tilted position by the locking pins during maintenance or service, posing a crush hazard.
- Unclassified
Consumer Product Recall · February 6, 2025
Sling CarriersThe recalled sling carriers violate the federal safety regulations for sling carriers, including requirements for structural integrity and occupant retention, posing a fall hazard to babies.
- Unclassified
Consumer Product Recall · February 6, 2025
Thy Trading Company, of Phoenixville, Pennsylvania
Roll Up Window BlindsThe recalled window blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window blinds are in violation of the federal regulations for window coverings and present a substantial product hazard.
- Unclassified
Consumer Product Recall · February 6, 2025
TTI Outdoor Power Equipment Inc., of Anderson, South Carolina
RYOBI 40-Volt Brushless 21" Cordless Walk-Behind MowersThe recalled mowers have a push-on connector inside the powerhead that can overheat, posing a fire hazard.
- Class II
Food Recall · February 5, 2025
Feel Good Foods; Three Cheese Mac & Cheese Bites; NET WT 8oz (224g); packaged in yellow carton; 9 units per case; Frozen; UPC: 89903900280-8Foreign object (metal pieces).
- Class I
Medical Device Recall · February 5, 2025
Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLUnexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not identified and used - stroke (reversible and irreversible).
- Class I
Medical Device Recall · February 5, 2025
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAXThere is the potential for missing motor mounting screws, which may have occurred during the servicing process.
- Class II
Food Recall · February 5, 2025
Organic Acai Bowl with berries, bananas, granola and dried coconut; Net Wt. 10 oz (284g); Frozen storage; Packaged in paper bowl with heat-sealed plastic filmPotential contamination with blue pieces of plastic
- Class I
Medical Device Recall · February 5, 2025
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
- Unclassified
Vehicle Recall · February 5, 2025
2023 ALTEC AERIAL DEVICEA fuel leak in the presence of an ignition source can increase the risk of a fire.
- Class II
Medical Device Recall · February 5, 2025
INTELERAD MEDICAL SYSTEMS INCORPORATED
IntelePACS (Image Fusion Module) - InteleViewerA software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on the days of Daylight Savings Time (DST); only on dates in which DST transition occurs; all other dates are unaffected. An incorrect SUV may lead to an incorrect diagnosis.
- Class II
Medical Device Recall · February 5, 2025
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137.the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.
- Unclassified
Vehicle Recall · February 5, 2025
2025 FOREST RIVER CAMPSITE RESERVEWiring without circuit protection may become damaged and short circuit, increasing the risk of a fire.
- Unclassified
Vehicle Recall · February 5, 2025
2025 MERCEDES-BENZ C 300A loose seat belt may not properly restrain an occupant during a crash, increasing the risk of injury.
- Class I
Medical Device Recall · February 5, 2025
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix facture/break could cause vessel injury and lead to severe bleeding.
- Class II
Medical Device Recall · February 5, 2025
Medical Information Technology, Inc.
MEDITECH Expanse Laboratory (LAB), Microbiology (MIC), Anatomical Pathology (PTH), Genetics (GEN). Calculator/data processing module for clinical use.Entering multiple keys that trigger input simultaneously may remove data from first field of screens and/or questionnaires with more than one field.
- Class II
Medical Device Recall · February 5, 2025
Access 2 Immunoassay Analyzer, Catalog Number 81600NBeckman Coulter identified that an issue for Access 2 Sample Motors (B48016) due to improper alignment, causing the motors to rub against the sample wheelbase plate and index sensor. The issue was traced to a worn tool used in production (at the supplier), affecting Access 2 sample motors. This could lead to a potential delay in reporting patient test results.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Trader Joe's branded Solid White Albacore Tuna in olive oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 99287Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Van Camp's branded Solid Light Yellowfin in Vegetable oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Distributed by: Chicken of The Sea Intl.; El Segundo, CA 90245 U.S.A. UPC# 48000 25015 UPC# 48000 7Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Trader Joe's branded Solid White Albacore Tuna in Water, salt added; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 0099285Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Trader Joe's branded Solid White Albacore Tuna in water, Low sodium; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 95836Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Genova branded Yellowfin Tuna; Genova; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 73265 UPC# 48Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Trader Joe's branded Solid Light Yellowfin Tuna in olive oil, Pole & Line Caught; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 51403Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Food Recall · February 4, 2025
Chicken of the Sea; Thai Union
Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and Sea Salt; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 13275Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.
- Class II
Medical Device Recall · February 4, 2025
CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.During an internal investigation, ACS was unable to confirm that the CODMAN component achieved the required Sterility Assurance Level and therefore is not suitable for sterilization according to ACS procedures.
- Class II
Medical Device Recall · February 4, 2025
IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit; UPN/Catalog Number: ISO-60;Product is mislabeled with the incorrect fill volume.
- Class II
Food Recall · February 4, 2025
Item #96522, King Harvest Lemon Hummus, net wt. 10oz., UPC 025726 31001 1, perishable and refrigerated, packed in sealed plastic tub and lid. Exclusively by Pacific Coast Fresh Co Portland, Oregon.Plastic fragments