Safety Recalls
RSS ↗15,259 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,101–5,150 of 15,259
- Class I
Medical Device Recall · August 8, 2025
Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701BConvenience kits labeled as sterile have not gone through the sterilization process.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 9B, Software Version: 9.1.0.933. 2. RayStation 9B Service Pack 1, Software Version: 9.2.0.483. 3. RayStation 10A, Software VDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 11B, Software Version: 12.0.0.932. 2. RayStation 11B Service Pack 1, Software Version: 12.1.0.1221. 3. RayStation 11B ServicDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 8B, Software Version: 8.1.0.47. 2. RayStation 8B Service Pack 1, Software Version: 8.1.1.8. 3. RayStation 8B Service Pack 2,DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Unclassified
Vehicle Recall · August 8, 2025
2025 FORD MUSTANG, 2025 LINCOLN NAUTILUSExterior lighting failure can reduce visibility for the driver and other road users, increasing the risk of a crash.
- Unclassified
Vehicle Recall · August 8, 2025
2024 FORD MUSTANGAn instrument panel display that does not show critical information, such as warning lights or vehicle speed, increases the risk of a crash.
- Class II
Drug Recall · August 8, 2025
Glenmark Pharmaceuticals Inc., USA
Theophylline extended-release tablets 400mg, 100-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited, Colvale-Bardez, Goa- 403513 India, Manufactured for: Glenmark PharmaceuticalsFailed Dissolution Specifications: Failure results (above) were reported for the Dissolution (by UV) test for commercial annual stability at the long-term shelf life stability interval, wherein the dissolution results do not comply with L3 stage dissolution criteria.
- Unclassified
Vehicle Recall · August 8, 2025
2024 LINCOLN NAUTILUS, 2025 LINCOLN NAUTILUSA closing window may exert excessive force by pinching a driver or passenger before retracting, increasing the risk of injury.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 2023B, Software Version: 14.0.0.3338. 2. RayStation 2024A, Software Version: 15.0.0.430. 3. RayStation 2024A SP3, Software VDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 7, Software Version: 7.0.0.19. 2. RayStation 8A, Software Version: 8.0.0.61. 3. RayStation 8A Service Pack 1, Software VersiDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class II
Drug Recall · August 8, 2025
Breckenridge Pharmaceutical, Inc.
Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000 Capsules per bottle, Rx Only, Manufactured by: Towa Pharmaceutical Europe, S.L., Martorelles, (Barcelona), Spain. Manufactured for: Quallent PhaCGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 11A, Software Version: 11.0.0.951. 2. RayStation 11A Service Pack 1, Software Version: 11.0.1.29. 3. RayStation 11A ServiceDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 6 Service Pack 1, Software Version: 6.1.1.2. 2. RayStation 6 Service Pack 2, Software Version: 6.2.0.7. 3. RayStation 6 ServDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class I
Medical Device Recall · August 8, 2025
Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038BConvenience kits labeled as sterile have not gone through the sterilization process.
- Class II
Medical Device Recall · August 8, 2025
RayStation with the following product descriptions: 1. RayStation 12A, Software Version: 13.0.0.1547. 2. RayStation 12A Service Pack 1, Software Version: 13.1.0.144. 3. RayStation 12A ServicDICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the interface to Accuray's iDMS, are not guaranteed to be unique.
- Class III
Medical Device Recall · August 7, 2025
Flosonics Medical (R/A 1929803 ONTARIO CORP.)
FloPatch FP120, REF: FP120-FOT01-005Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.
- Unclassified
Consumer Product Recall · August 7, 2025
La Ligne Enfant Bonne Nuit PajamasThe recalled children's pajama sets violate mandatory standards for children's sleepwear flammability, posing a risk of burn injuries to children.
- Unclassified
Consumer Product Recall · August 7, 2025
Doskocil Manufacturing Company Inc., dba Petmate, of Arlington, Texas
Pet Zone Laser Pointer & LED Ball Pet ToysThe recalled pet toys violate the mandatory standard for consumer products containing button cell or coin batteries as required by Reese's Law because the LED-illuminated plastic sphere can break upon impact, making the button cell batteries easily accessible to children, posing an ingestion hazard. Swallowed batteries can cause serious injuries, internal chemical burns and death.
- Unclassified
Consumer Product Recall · August 7, 2025
Shan tou shi bei bei jia mao yi you xian gong si dba TEMI Toys, of China
TEMI Go Basketball ToysThe recalled toy contains small balls and is intended for children under three years of age, which violates the small ball ban, posing a deadly choking hazard.
- Class II
Food Recall · August 7, 2025
Cajun Seasoning (Taratino) NET WT: 50 lb Usage: 13.80 LBS for 300 LBS of Meat UPC (QST# 4546)Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
- Class II
Drug Recall · August 7, 2025
Glenmark Pharmaceuticals Inc., USA
Carvedilol Tablets, USP, 12.5 mg, 500-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd, Colvale-Bardez, Goa, 403513, India. Manufactured for Glenmark Pharmaceuticals, Inc., USA, MaCGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
- Class II
Drug Recall · August 7, 2025
Glenmark Pharmaceuticals Inc., USA
Carvedilol Tablets, USP, 3.125 mg, Packaged as: a)500-count bottle, NDC 68462-162-05; b) 100-count bottle, NDC 68462-162-01; Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd, Colvale-Bardez, GoaCGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
- Unclassified
Consumer Product Recall · August 7, 2025
Monica Vinader Inc., of New York, New York
Monica Vinader 14k Yellow Gold Mini Heart JewelryThe jewelry can contain excess levels of cadmium, which can be toxic if ingested by young children and may cause adverse health effects through long-term skin exposure.
- Class II
Food Recall · August 7, 2025
(Bulk) Oyster, Frozen, Raw Half Shell, 15lb(6.8kg) UPC: 10087703078342 Harvest Dates: Jan 03,2025, Jan 14,2025Oyster product potentially contaminated with Norovirus
- Class II
Food Recall · August 7, 2025
BBQ Riblet Seasoning (Cargill Meat)(PPM) NET WT: 50 lb UPC (QST# 5275)Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
- Unclassified
Consumer Product Recall · August 7, 2025
Tech Gear 5.7 Inc., dba Fieldsheer Apparel Technologies, of Carlsbad, California
Fieldsheer Heated SocksThe socks can cause pain and discomfort resulting in burns and blisters when worn during high-intensity activities that generate a combination of heat, excessive friction, moisture and pressure, posing an injury hazard.
- Class II
Food Recall · August 7, 2025
Reduced Sodium Roast Beef Rub (Serv-Rite) NET WT: 50 lb UPC (QST# 6313)Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
- Class II
Drug Recall · August 7, 2025
Glenmark Pharmaceuticals Inc., USA
Carvedilol Tablets, USP, 25 mg, 500-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd, Colvale-Bardez, Goa, 403513, India. Manufactured for Glenmark Pharmaceuticals, Inc., USA, MahwCGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
- Class II
Food Recall · August 7, 2025
Lemon Pepper Seasoning (Tarantino) NET WT: 50 lb UPC (QST# 6402)Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
- Unclassified
Consumer Product Recall · August 7, 2025
AliExpress, of San Mateo, California
LeymanKids Children's Pajama SetsThe recalled children's pajama sets violate the mandatory flammability standards for children's sleepwear, posing a risk of burn injuries or death to children.
- Unclassified
Consumer Product Recall · August 7, 2025
Deale International LLC, of Fort Lauderdale, Florida
Altafit af28 SmartwatchesThe smartwatch's wireless charging pad can overheat and ignite, posing a risk of serious burn injury and fire hazard.
- Unclassified
Consumer Product Recall · August 7, 2025
Guangzhou Ariel Biotech Co. Ltd., of China
Séfralls Minoxidil Hair Generation SerumThe hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.
- Class III
Food Recall · August 6, 2025
HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17Unapproved Drug Claims.
- Class III
Food Recall · August 6, 2025
HI-TECH PHARMACEUTICALS BETA SITOSTEROL (715MG PINE DERIVED PHYTOSTEROL 99%) PROVIDES SUPPORT FOR OVERALL CARDIOVASCULAR HEALTH HELPS MAINTAIN HEALTHY CHOLESTEROL LEVELS ALREADY WITHIN THE NORMAL RANGUnapproved Drug Claims and Misbranded.
- Class II
Food Recall · August 6, 2025
English Toffee, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, packed in flexible plastic bagAllergen labeling: specific tree nut (pecans) not listed in the 'contains' statement
- Class III
Food Recall · August 6, 2025
IFN iFORCE NUTRITION JOINT HELP HEALTHY JOINTS & LIGAMENTS DIETARY SUPPLEMENT 120 CAPSULES UPC 8 54503 00226 5 Manufactured By: iForce Nutrition 6015B Unity Drive Norcross, GA 30071Unapproved Drug Claims.
- Class II
Drug Recall · August 6, 2025
Glenmark Pharmaceuticals Inc., USA
Carvedilol Tablets, USP, 25 mg, 500 Tablets per carton, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot No. 2, Phase-2, Pharma Zone SEZ, Pithampur, Dist.-Dhar, Madhya Pradesh 454 775, InCGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
- Class II
Medical Device Recall · August 6, 2025
Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test kit: A collection of reagents and other associated materials intended to be usAs a result of Post-Market half-time stability testing, false negative test result was observed for a positive sample type.
- Class II
Food Recall · August 6, 2025
Peanut Butter Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshellAllergen labeling: egg not listed in the 'contains' statement
- Class II
Medical Device Recall · August 6, 2025
Smiths Medical CADD" Yellow Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included 100mL, Product Code 21-7300-24Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
- Class I
Medical Device Recall · August 6, 2025
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110The catheters may not retain their shape.
- Class II
Medical Device Recall · August 6, 2025
Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included. 50mL, Product Code 21-7001-24Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
- Class III
Food Recall · August 6, 2025
PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT KIWI-STRAWBERRY NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUnapproved Drug Claims and Misbranded.
- Class II
Food Recall · August 6, 2025
Pecan Toffee Clusters, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 5oz, flexible plastic bagAllergen labeling: specific tree nut (pecan) not listed in 'contains' statement
- Class II
Food Recall · August 6, 2025
Chocolate Mint Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshellAllergen labeling: egg is not listed in the 'contains' statement
- Class III
Food Recall · August 6, 2025
HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity DrUnapproved Drug Claims.
- Class III
Food Recall · August 6, 2025
HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST AND SECRETAGOGUES NOVEL GIP (GLUCOSE-DEPENDENT ISNULINOTROPIC POLYPEPTIDE) RECEUnapproved Drug Claims and Misbranded.
- Class II
Food Recall · August 6, 2025
Maple Nut Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshellAllergen labeling: specific tree nut (pecan) and egg not listed in 'contains' statement
- Class II
Food Recall · August 6, 2025
Chocolate Pecan Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshellAllergen labeling: specific tree nut (pecan) and egg are not listed in the 'contains' statement
- Class III
Food Recall · August 6, 2025
PRIMENUTRITION PHYTOFORM FRUITS & GREENS FORMULA 30 SERVINGS DETOXIFICATION IMPROVE ENERGY SWEETENED WITH MONK FRUIT WATERMELON NATURALLY & ARTIFICIALLY FLAVORED NET WT 13.75 OZ (390g) DIETARY SUPPLEUnapproved Drug Claims and Misbranded.