Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,401–11,450 of 15,364
- Class II
Food Recall · June 21, 2024
"THE PERFECT CHOCOLATE CHUNK COOKIE MIX Cravings by Chrissy Teigen NET WT. 15.76 OZ (447g)" Packaged in a beige cardboard box, with green letteringUndeclared allergen - coconut
- Class I
Food Recall · June 20, 2024
1. Greens Solata 5050; 6x10 clamshell; UPC: 850021494766 / 2. Greens Gaia Organic 5050; 6x10 clamshell; UPC: 850021494827 / 3. Greens Gaia Organic 50/50 blend; 8x45 clamshell; UPC: 850021494919 / 4.Product may be contaminated with Listeria monocytogenes.
- Unclassified
Consumer Product Recall · June 20, 2024
StyleCraft LLC, of Boca Raton, Florida
Instinct Professional Vector Motor Cordless Hair ClippersThe lithium-ion battery in the recalled clippers can overheat, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · June 20, 2024
JiuDing Tools Co. Ltd., of China
Theefun Kids Gardening Tools SetsThe brown handle strings contain levels of phthalates that exceed the federal phthalate ban. Phthalates are toxic if ingested by young children and can cause adverse health effects.
- Class I
Food Recall · June 20, 2024
1. Greens Solata Spinach; 10x9 bag; UPC: 854311007391 / 2. Greens Full Circle Organic Baby Spinach; 6x10 Clamshell; UPC: 036800490512 / 3. Greens Solata Baby Spinach 6x10 clamshell; UPC: 85002149475 /Product may be contaminated with Listeria monocytogenes.
- Unclassified
Consumer Product Recall · June 20, 2024
Global Homes USA, of Charlotte, North Carolina
Cedona Natural View six-drawer dressersThe 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 do not comply with the performance requirements of the STURDY Act.
- Unclassified
Consumer Product Recall · June 20, 2024
Vita-Mix Corporation, of Cleveland, Ohio
Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade BasesThe containers can separate from the blade base, exposing the blades, posing a laceration hazard to consumers.
- Unclassified
Consumer Product Recall · June 20, 2024
Babboe B.V., of the Netherlands
Cargo bicyclesThe frames of the recalled cargo bicycles can crack and can bend and break, posing a fall hazard to the rider.
- Unclassified
Consumer Product Recall · June 20, 2024
Cinmar LLC, of West Chester, Ohio
Frontgate Resort Collection Newport Aluminum and Teak ChaisesWhen adjusting the backrest while seated, the adjustable backrest can unexpectedly descend with force, posing finger crushing and amputation hazards.
- Class I
Food Recall · June 20, 2024
Deluxe Roasted Salted Mixed Nuts ITEM NUMBER 99651 UPC: 6-51433-99651-6 SELL BY: 10/09/2024Undeclared allergen; peanuts
- Class II
Medical Device Recall · June 20, 2024
Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.
- Class I
Food Recall · June 20, 2024
1. Greens Full Circle Organic Power Greens; 6x10 Clamshell; UPC: 036800490550 / 2. Greens Gaia Organic Power Greens; 8x45 clamshell; UPC: 850021494889 / 3. Greens Full Circle Organic Power Greens; 8xProduct may be contaminated with Listeria monocytogenes.
- Class II
Food Recall · June 20, 2024
"feve x DANDELION CHOCOLATE CHOCOLATE - COVERED COCOA NIBS 4 OUNCES 113 GRAMS" Black triangular box with gold lettering. Black box contains cellophane bag.Undeclared allergen - hazelnuts
- Class II
Medical Device Recall · June 20, 2024
Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.This is a risk that alarms will not be received by the Arial Wireless Nurse Call System and premature depletion of the battery.
- Unclassified
Consumer Product Recall · June 20, 2024
Head Rush Technologies, of Louisville, Colorado
TRUBLUE iQ Auto Belay DevicesThe recalled auto belay device can fail to retract, posing a fall hazard and risk of serious injury or death.
- Class II
Medical Device Recall · June 20, 2024
Cepheid, Sample Collection Device, Part: 900-0370Specimen collection device may leak after the patient sample swabs have been inserted into the test tubes, which could result in biohazard exposure, cross contamination causing false positive results for other specimens, and/or delay to test results.
- Class I
Food Recall · June 20, 2024
1. Greens Gaia Organic Spring Mix; 6x1.7 clamshell; UPC: 850039434075 / 2. Greens Gaia Organic Spring Mix; 6x1.7 clamshell; UPC: 850039434082 / 3. Greens Full Circle Organic Spring Mix; 6x10 clamshellProduct may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · June 20, 2024
1. Greens Gaia Organic Spring Mix Herb; 8x45 clamshell; UPC: 850021494896 / 2. Greens Solata Spring Mix Herb; 8x5 clamshell; UPC: 854311007063 / 3. Greens Uncle Vinny's Spring Mix Herb; 8x5 clamshellProduct may be contaminated with Listeria monocytogenes.
- Class I
Food Recall · June 20, 2024
1. Greens Farmer Direct Organic Chopped Kale Spinach; 6x9 bag; UPC: 854311007377 /Product may be contaminated with Listeria monocytogenes.
- Class II
Medical Device Recall · June 20, 2024
Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid TestPotential for defective test cartridges which may result in false positive results for the Staphylococcus lugdunensis and Enterococcus faecium targets.
- Unclassified
Consumer Product Recall · June 20, 2024
Goal Zero LLC, of Draper, Utah
Yeti Link Expansion Modules and EC8 CablesThe connection between the Yeti Link Expansion modules and the cables can overheat and melt, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · June 20, 2024
JoyJolt Drinkware Declan Single-Wall Glass Coffee MugsThe glass mugs can break and crack when filled with hot liquids, posing burn and laceration hazards.
- Unclassified
Consumer Product Recall · June 20, 2024
CBOCS Distribution Inc., of Lebanon, Tennessee
Lavender scented candles in a round wooden bread bowlThe candle's flames can reach excessive heights and can ignite the bowl, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · June 20, 2024
RFA Brands LLC, d/b/a myCharge, of Birmingham, Michigan
myCharge POWER HUB All-In-One 10,000mAh portable chargersThe recalled portable chargers can overheat while charging, posing fire and burn hazards.
- Class I
Food Recall · June 19, 2024
Terrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g)Product tested positive for presence of salmonella.
- Class II
Food Recall · June 19, 2024
C. Kreuger Gluten Free Peanut Butter Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for 30 days at ambient and 1 year frozen.No ingredient statement on the label.
- Class II
Food Recall · June 19, 2024
C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for 30 days at ambient and 1 year frozen.No ingredient statement on the label.
- Class II
Medical Device Recall · June 19, 2024
UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-038Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
- Class II
Medical Device Recall · June 19, 2024
UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-043Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
- Class II
Medical Device Recall · June 19, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY Systems, when used in conjunction with Culture Media Bottles: BACT/ALERT FA PLUS, REF: 410851, and BACT/ALERT PFIf blood culture identification panel is used in conjunction with specific lots of culture media bottles, then false positive Serratia marcescens results may occur, due to an increased level of non-viable organism from serratia marcescens targets in culture media bottles, false positive result may lead to an inappropriate change in patient therapy.
- Class II
Medical Device Recall · June 19, 2024
UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-042Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
- Class II
Drug Recall · June 18, 2024
Fresenius Medical Care Holdings, Inc.
DELFLEX PERITONEAL DIALYSIS SOLUTION With LOW MAGNESIUM / LOW CALCIUM 4.25% DEXTROSE and attached stay "safe Exchange Set, 2500mL (Approx. 50 mL excess), Single Dose Container Sterile and Non-PyrogeniThis product is being recalled due to the tube weld failure presents itself as a slow leak and can be difficult to detect.
- Class II
Food Recall · June 18, 2024
Universal Bakery Organic Sunrise Energy Bars 32 oz. and 10 oz. Gluten Free USDA Organic Made With: Rolled Oats, Dried Fruits, Flax Seeds, Quinoa, Coconut, Pumpkin Seeds, Chia Seeds + More IngredientPotential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
- Class II
Drug Recall · June 18, 2024
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card in one carton, Rx only, Mfg by: Cadila Healthcare Ltd., Ahmedabad, India, Distributed by: Major Pharmaceutical 1Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.
- Class III
Drug Recall · June 18, 2024
Dodex Injectable (Cyanocobalamin Injection) USP, 1,000mcg/mL, 1mL multiple dose vial, Rx only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals LimitSubpotent drug: out of specification results
- Class II
Medical Device Recall · June 18, 2024
MEDLINE INDUSTRIES, LP - Northfield
KIT PEDI CRANI LAMI, Pack Number DYNJ907372AA non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
- Class II
Medical Device Recall · June 18, 2024
MEDLINE INDUSTRIES, LP - Northfield
CRANIOTOMY PACK, Pack Number DYNJ46552OA non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
- Class II
Medical Device Recall · June 18, 2024
MEDLINE INDUSTRIES, LP - Northfield
ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes sterility during its use, there is an increased risk of patient infection.
- Class II
Medical Device Recall · June 18, 2024
FoundationOne Companion Diagnostic (F1CDx)Two (2) reports were sent to customers with an incorrect negative claim on the claims page; the device variant information was displayed correctly in the tumor profiling section of both FDA-approved test reports.
- Class II
Medical Device Recall · June 18, 2024
SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732701Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
- Class II
Medical Device Recall · June 18, 2024
SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
- Class II
Food Recall · June 18, 2024
Principal Display: SureLife Foods PALEO BARS, Net Wt. 14 oz. (392 g.)- 14 ct. individually wrapped bars (28 g. each) Certified Gluten Free, Certified Paleo Loaed with: Almonds, Honey, Shredded CoconPotential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.