Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,451–7,500 of 15,271
- Class II
Medical Device Recall · March 18, 2025
Automated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1¿(German/English dual language), DCF-E2310E3/1¿(German/French dual language), DCF-E2310F3/1¿ (French/English dual languageIt was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).
- Class II
Food Recall · March 18, 2025
Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's, Net Weight: 22.5oz. (638g), 5 units per package, Vacuum seal packages and twist tie bags, KEEP REFRIGERATED. UPC 850283002037Undeclared allergen: Soy lecithin, less than 2%
- Class II
Medical Device Recall · March 18, 2025
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software versions Product Description: CELL-DYN Ruby Component: NoWhen expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use of expired reagents is against the guidelines of the Operator's Manual.
- Class II
Medical Device Recall · March 18, 2025
Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-E110SG-DE/1 (German language), DCF-E110SG-FR/1 (French language), DCF-E110SG-IT/1 (Italian language)It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).
- Class II
Food Recall · March 18, 2025
Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)Potential contamination with patulin.
- Class II
Medical Device Recall · March 18, 2025
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw, and exchange may exceed 30 minutes.
- Class II
Medical Device Recall · March 18, 2025
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-10 Software Version: All software versions Product Description: CELL-DYN Ruby Component: NoWhen expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use of expired reagents is against the guidelines of the Operator's Manual.
- Class II
Medical Device Recall · March 18, 2025
Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual language)It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).
- Class II
Medical Device Recall · March 18, 2025
Automated External Defibrillators, Model DDU-2450. Item number: DCF-E2460DE (German language)It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).
- Class II
Medical Device Recall · March 18, 2025
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-13 Software Version: All software versions Product Description: CELL-DYN Ruby Component: NoWhen expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use of expired reagents is against the guidelines of the Operator's Manual.
- Class II
Medical Device Recall · March 18, 2025
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 04U42-84 Software Version: All software versions Product Description: CELL-DYN RubyWhen expired reagents are scanned or manually entered, the system will change the expiration date to current or future date without notifying user that an expired reagent is being used. Use of expired reagents is against the guidelines of the Operator's Manual.
- Class II
Medical Device Recall · March 17, 2025
Amplatzer TorqVue LP Catheter (TVLPC), Model no. 9-TVLPC4F90/080Device may have a small breach in the proximal end of the shaft under the strain relief of the delivery system. Breach is not visibly detectable and may lead to prolonged procedure, blood loss, or air ingress with potential for air embolism.
- Class II
Food Recall · March 17, 2025
GOLD GARLIC POWDER IRRADIATED; NET WT. 50 LBS; PRODUCT OF CHINAPotential contamination with foreign objects (metal)
- Class II
Food Recall · March 17, 2025
Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case)Misbranded - label states 2g total carbohydrates instead of 27g
- Class II
Food Recall · March 17, 2025
Nestle-USA, Inc. (Corporate Office)
Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per casePotential foreign material (wood-like material)
- Class II
Medical Device Recall · March 17, 2025
Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080Device may have a small breach in the proximal end of the shaft under the strain relief of the delivery system. Breach is not visibly detectable and may lead to prolonged procedure, blood loss, or air ingress with potential for air embolism.
- Class II
Food Recall · March 17, 2025
Nestle-USA, Inc. (Corporate Office)
Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per casePotential foreign material (wood-like material)
- Class II
Drug Recall · March 17, 2025
Atorvastatin Calcium Tablets USP 40 mg, 1000-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009 USA, Manufactured by: Recipharm Pharmaservices PVT, Ltd Bengaluru, INDIAFailed dissolution specifications: lower than specifications
- Class II
Medical Device Recall · March 17, 2025
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 Software versions: V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3 The Beckman Coulter DxCThe reason for the recall is incorrect sample barcode identification and processing errors that result in the reporting of erroneous and delayed results.
- Class II
Food Recall · March 17, 2025
Nestle-USA, Inc. (Corporate Office)
Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per casePotential foreign material (wood-like material)
- Class II
Food Recall · March 17, 2025
Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benzoate), water, sugar, cooking wine( water, rice, malt), sweet cooking wine(corn syrup, rice, water, mShelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.
- Class I
Food Recall · March 14, 2025
Jinga Glass Noodles with vegetables 8 oz. and 12 oz.Contains undeclared egg
- Class II
Medical Device Recall · March 14, 2025
Merit Medical , REF: R2275, EsophyX Z+ with SerosaFuse Implantable Fasteners, (1) Fastener Delivery Device, (2) 7.5mm Cartridges, STERILEEO,RxOnlyUpdate to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.
- Class II
Medical Device Recall · March 14, 2025
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the casing near the cable.
- Class II
Medical Device Recall · March 14, 2025
DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)Potential of compromised compatibility resulting in influence on the positioning of the reference array and an influence of the function of the navigation system cannot be excluded.
- Class II
Medical Device Recall · March 14, 2025
Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnlyUpdate to IFU to provide additional information related to risk with device over-rotation and multiple deployment of fasteners.
- Class I
Medical Device Recall · March 13, 2025
HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with HeartMate 3 and II Left Ventricular Assist System.Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical component that may cause MPU not to turn on, unprompted shut down, or turning off/restarting, may cause system controller to indicate Yellow Wrench or No External Power alarms. If MPU losses power, System Controller can support the pump up to 15 minutes, and if not switched to rechargeable batteries, pump may lose power.
- Unclassified
Consumer Product Recall · March 13, 2025
Black Diamond Equipment Ltd., of Salt Lake City, Utah
BD Vision Climbing HarnessThe recalled BD Vision harnesses can degrade over time and fail to support the climber, posing a fall hazard resulting in serious injury or death.
- Unclassified
Consumer Product Recall · March 13, 2025
Sublue Technology Inc., of Walnut, California
Sublue Mix underwater scooters and replacement batteries (black batteries only)The lithium-ion batteries can overheat and ignite, posing a fire hazard to consumers.
- Class I
Drug Recall · March 13, 2025
Dr. Reddy's Laboratories, Inc.
Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured by: Gland Pharma Limited, Hyderabad, - 500 043 INDIA, Distributor: Dr. Reddy's LaboratorieLABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL, while the aluminum overwrap packaging correctly identifies the product as Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL.
- Class II
Medical Device Recall · March 13, 2025
Brand Name: Celsior Cold Storage Solution Product Name: Celsior Cold Storage Solution Model/Catalog Number: 533682 Product Description: In US Celsior is a class II medical device. Celsior is a cleaThe potential for risk of microbiological contamination of products due to inability to ensure sterility assurance throughout aseptic manufacturing.
- Class II
Food Recall · March 13, 2025
La Mexicana Tortilla Factory, Inc.
Tortilla Chip Green 4 cut packed 5lbs per bag; 6 bags per boxUndeclared Yellow #5