Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,601–7,650 of 15,271
- Unclassified
Vehicle Recall · March 6, 2025
2025 HYUNDAI IONIQ 5Improperly aimed headlights can result in insufficient illumination of the road, decreasing the driver's visibility and increasing the risk of a crash.
- Class II
Drug Recall · March 6, 2025
fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 mL (1.25 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For ILack of Assurance of Sterility
- Unclassified
Vehicle Recall · March 6, 2025
2025 FORD EXPLORERLoss of brake function and wheel damage can increase the risk of a crash.
- Class II
Medical Device Recall · March 6, 2025
Pacific Hemostasis Thromboplastin-D, 10 ml. Used in performing one-stage prothrombin time test and factor assays.The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
- Unclassified
Consumer Product Recall · March 6, 2025
Luv n' care, of Monroe, Louisiana
Nuby Stroller FansThe stroller fan's housing allows consumers' fingers to contact the fan's blade, posing a laceration injury hazard to small children.
- Unclassified
Consumer Product Recall · March 6, 2025
Black Diamond Equipment Ltd., of Salt Lake City, Utah
BD Recon LT Avalanche TransceiversThe metal contact in the switch mechanism of the Recon LT avalanche transceiver can corrode and cause the transceiver to malfunction. If this occurs, the device can turn off and make it impossible to locate a victim in an avalanche, which could result in serious injury or death.
- Unclassified
Consumer Product Recall · March 6, 2025
Nanchang Zhongcangjishi E-commerce Co. Ltd, of China
Lolanta Children's BathrobesThe recalled children's bathrobes violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries and death to children.
- Unclassified
Consumer Product Recall · March 6, 2025
Shenzhen Comfort Dream Home Textiles Co. LTD, dba Love Our Home, of China
Love Our Home Braided Crib BumpersThe recalled crib bumpers violate the federal crib bumper ban, posing a deadly suffocation hazard to infants. Padded crib bumpers are banned by the federal Safe Sleep for Babies Act.
- Unclassified
Consumer Product Recall · March 6, 2025
Round 2 LLC, of South Bend, Indiana
Auto World Unassembled Deluxe Pit Kit Slot CarsThe recalled unassembled Deluxe Pit Kit slot cars violate the mandatory federal regulation for magnets because the magnets used to power the car are loose prior to assembly, posing an ingestion hazard to children. Assembled models do not pose this risk and are therefore not subject to this recall. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Instrument Check Block, Catalog Number MRUE203, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Glenoid Box Lid, Catalog Number MRUE205, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Drug Recall · March 5, 2025
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless Steel, Catalog Number MRUE200, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total ShoulStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Drug Recall · March 5, 2025
La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube,cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
- Class II
Medical Device Recall · March 5, 2025
HiResolution" Bionic Ear System - M Battery Charger Model Number CI-5607Due to incorrect the battery charger being packaged and distributed. Product labeling does not match the intended product as specified.
- Class II
Medical Device Recall · March 5, 2025
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720RMedline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
- Class II
Drug Recall · March 5, 2025
Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000-count bottle, Rx only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC 57237-018-99CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Drug Recall · March 5, 2025
Golden State Medical Supply Inc.
PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, CA 93012 NDC 51407-444-30Failed Dissolution Specifications
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Box Base, Catalog Number MRUE204, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Drug Recall · March 5, 2025
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, NewChemical Contamination: This recall has been initiated due to detected trace levels of benzene.
- Class II
Food Recall · March 5, 2025
Golden Crop Candy (8 oz. (227g) un-wrapped candies)Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
- Class II
Medical Device Recall · March 5, 2025
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980RMedline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Food Recall · March 5, 2025
Golden Crop Candy (10 oz. (283g) wrapped candies)Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
- Class II
Medical Device Recall · March 5, 2025
stryker HoloBlueprint Application, Catalog Number MRUE001; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Drug Recall · March 5, 2025
Testosterone Gel 1%, 5 grams, 30 Unit-dose Packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-152-02Presence of foreign substance: Presence of Benzene.
- Class II
Drug Recall · March 5, 2025
Testosterone Gel 1%, 2.5 grams, 30 Unit-dose packets in a carton, Rx only, Distributed by: Strides Pharma Inc., East Brunswick, NJ, NDC 64380-151-02Presence of foreign substance: Presence of Benzene.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in stryker Blueprint Mixed Reality Instrument Kit, Catalog Number MRUEGLN; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Medical Device Recall · March 5, 2025
stryker Blueprint Mixed Reality Depth Stop Pin, Catalog Number MRUE206; Total Shoulder ArthroplastyStryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
- Class II
Medical Device Recall · March 5, 2025
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP,w/Integrated Cable (Blue/Grey), Number REF EICA58740RMedline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
- Class II
Medical Device Recall · March 5, 2025
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand,w/Integrated Saline Line & Integrated Cable, Item Number REF EICA58720RMedline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
- Class II
Drug Recall · March 4, 2025
Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg, Nighttime Sleep-Aid, 4 x 8 blister packs per carton, Cherry flavor, Manufactured by Adare Pharmaceuticals, Inc., Dist. by Chattem, Inc., P.O. BoCGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the daily acceptable intake limit defined by the Food and Drug Administration.
- Class II
Medical Device Recall · March 4, 2025
Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F, SterileEO, Rx Onlyproduct mix-up; Vascular stent labeled as one size but contains a different size.
- Class II
Food Recall · March 4, 2025
Panang Curry Tofu Vegan GF is a refrigerated and ready to eat product, packaged in plastic box, net wt. 13.5oz. UPC 88581 149928. Label declares ingredients as Tofu, Panang Curry Paste, Carrots and PLabel declares tofu but it does not declare soy.
- Class III
Food Recall · March 4, 2025
BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.Product contains cyclamates
- Class II
Medical Device Recall · March 4, 2025
Cordis, REF C10040ML, Smart Control Vascular Stent System ILIAC, 10mm X 40mm 6F, SterileEO, Rx Onlyproduct mix-up; Vascular stent labeled as one size but contains a different size.
- Class II
Medical Device Recall · March 4, 2025
InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNAInsulin pens may have been incorrectly assembled therefore users could experience the following: either the insulin cartridge will not fit into the cartridge holder; or the cartridge holder may be difficult to remove from the insulin pen. If the issue is present, and if the user does not have backup insulin they may experience temporary hyperglycemia.
- Class II
Medical Device Recall · March 4, 2025
Abbott Diagnostics Scarborough, Inc.
Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 435-000 Software Version: N/A Product Description: Respiratory virus panel nucleic acid assay system Component: NoThe impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
- Class II
Medical Device Recall · March 4, 2025
Abbott Diagnostics Scarborough, Inc.
Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software Version: N/A Product Description: Influenza A And Influenza B Multiplex Nucleic Athe impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
- Class II
Medical Device Recall · March 4, 2025
Abbott Diagnostics Scarborough, Inc.
Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software Version: N/A Product Description: Influenza A And Influenza B Multiplex Nucleic AThe impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
- Class III
Drug Recall · March 4, 2025
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
Tolterodine Tartrate Extended-Release Capsules, 2 mg, 30 Capsules (3 x 10) Unit Dose carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6592-04.Failed Dissolution Specifications: Out of specification results obtained during routine stability testing for dissolution.
- Class II
Medical Device Recall · March 4, 2025
Stimulation RC Clinician Programmer Application, Model A71400, when used with the Inceptiv (Model 977119) and Intellis Pro (Model 977118) neurostimulatorsThere is a software issue that can permanently disable communication with an implantable neurostimulator (INS) when a specific intraoperative programming sequence is used.
- Class II
Food Recall · March 4, 2025
Dinstuhl's Fine Candy Company, Inc.
Dinstuhl's Cashew Crunch, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Cashews, Coconut, Corn Syrup, Brown Sugar, Butter, Salt, Baking Soda.Undeclared allergen (milk)
- Class II
Food Recall · March 4, 2025
Dinstuhl's Fine Candy Company, Inc.
Dinstuhl's Peanut Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Corn Syrup, Baking Soda, Peanuts, Butter, Pure Vanilla Extract.Undeclared allergen (milk)
- Class II
Medical Device Recall · March 4, 2025
Abbott Diagnostics Scarborough, Inc.
Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 435-000 Software Version: N/A Product Description: Respiratory virus panel nucleic acid assay system Component: Nothe impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
- Unclassified
- Class II
Medical Device Recall · March 4, 2025
Abbott Diagnostics Scarborough, Inc.
Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 NucleThe impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.