Safety Recalls
RSS ↗17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 3,101–3,150 of 17,559
- Unclassified
Consumer Product Recall · March 12, 2026
ProRider, Inc., of Kent, Washington
ProRider Bicycle HelmetsThe recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- Unclassified
Consumer Product Recall · March 12, 2026
LFTE USA Inc., of Cary, North Carolina
Playground Swing Set SeatsThe rivets used to support the swing seat can fail, posing a fall hazard to children.
- Unclassified
Consumer Product Recall · March 12, 2026
Hong Kong Baojia International Limited, of China
17 Stories Furniture 14-Drawer DressersThe recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory standard as required by the STURDY Act.
- Class II
Food Recall · March 12, 2026
Western Mixers Produce & Nuts, Inc.
Chilli Spanish Peanuts, Treasured Harvest brand, 25lb clear plastic bag container. UPC:none Item code: 2608-25Foreign object (glass) found inside sealed container of finished product.
- Class III
Food Recall · March 12, 2026
Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml container. Packed in single serving, 3 units/pack, and 10 units per pack. Single UProduct does not meet label claim for Vitamin E.
- Class II
Food Recall · March 12, 2026
Western Mixers Produce & Nuts, Inc.
Chilli Spanish Peanuts, First Street brand, 11oz clear plastic container. UPC: None Item Code: 2608-T20Foreign object (glass) found inside sealed container of finished product.
- Class II
Medical Device Recall · March 11, 2026
ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 REF ASK-04020-EUH2 UDI code: (01)10801902213379(17)270731(11)251218(10)Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class II
Medical Device Recall · March 11, 2026
FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural CatheDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class II
Medical Device Recall · March 11, 2026
Windstone Medical Packaging, Inc.
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994AThe product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
- Class II
Drug Recall · March 11, 2026
5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-458-05, Unit of Sale NDC Number: 65219-4Lack of Assurance of Sterility
- Unclassified
Vehicle Recall · March 11, 2026
2025 VOLVO EX30, 2026 VOLVO EX30CCAn audible warning chime that does not properly alert of an unbelted seat belt can increase the risk of injury during a crash.
- Class II
Drug Recall · March 11, 2026
5% Dextrose Injection, USP 5 g per 100 mL (50 mg per mL) 100 mL in a 100 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-464-05, Unit of Sale NDC Number: 65219-464-Lack of Assurance of Sterility
- Class I
Food Recall · March 11, 2026
MILK WASH NET WEIGHT: 50OZ (1417g) Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, GA 30349Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
- Class II
Medical Device Recall · March 11, 2026
Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531(11)251205(10)33F25M0011 The Arrowg+ard technology is intended to provide proDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class I
Food Recall · March 11, 2026
Spray Dried Dairy Powder 25 kg bags or 1 metric ton totesSalmonella spp. identified in finished product testing
- Class II
Medical Device Recall · March 11, 2026
PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venousDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP 0.9% (450 mg per 50 mL) (9 mg per mL) 50 mL, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-466-05, Unit of SaleLack of Assurance of Sterility
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, (2,250 mg per 250 mL) (9 mg per mL) 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 6Lack of Assurance of Sterility
- Class II
Medical Device Recall · March 11, 2026
Windstone Medical Packaging, Inc.
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14433The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL) 500 mL in a Single Dose freeflex bag, 500 mL x 20, Manufactured for: Fresenius Kabi USA, LLC ("Fresenius Kabi"), IL 60047, Unit of ULack of Assurance of Sterility
- Class II
Medical Device Recall · March 11, 2026
Windstone Medical Packaging, Inc.
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
- Class I
Medical Device Recall · March 11, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06Reloads for curved-tipped stapler may potentially produce an incomplete staple line.
- Unclassified
Vehicle Recall · March 11, 2026
Aluminum Trailer Company (ATC)
2023 ATC PL700Exhaust fumes inside the cabin increase the risk of injury or death from carbon monoxide poisoning.
- Class II
Drug Recall · March 11, 2026
0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NLack of Assurance of Sterility
- Class II
Drug Recall · March 11, 2026
5% Dextrose Injection, USP 2.5 g per 50 mL (50 mg per mL) 50 mL in a 100 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-456-05, Unit of Sale NDC Number: 65219-456-Lack of Assurance of Sterility
- Class I
Food Recall · March 11, 2026
Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags Net Weight: 20lbs Allergy Information: CONTAINS: MILK, WHEAT Packed BY: Griffith Foods STONECREST, GA 30058Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
- Class II
Medical Device Recall · March 11, 2026
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-LumenDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class II
Medical Device Recall · March 11, 2026
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle protecDue to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 250 mL in a Single Dose freeflex bag, Rx only, BD Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417, DistributLack of Assurance of Sterility
- Class II
Medical Device Recall · March 11, 2026
ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-45703-MGH UDIDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 6Lack of Assurance of Sterility
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, 50 mL x60, Becton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, Distributed by BD, Manufactured by Fresenius Kabi USA, LLC ("Fresenius Kabi"Lack of Assurance of Sterility
- Unclassified
Vehicle Recall · March 11, 2026
Volkswagen Group of America, Inc.
2025 VOLKSWAGEN JETTAAn open circuit may draw a higher current and increase the risk of a fire.
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL), 1,000 mL in a Single Dose freeflex bag, Rx only, BD Becton, Dickson and Company, 1 Becton Drive, Franklin Lakes, NJ 07417, DistribuLack of Assurance of Sterility
- Class II
Food Recall · March 11, 2026
Horizon Organic Chocolate Organic Lowfat Milk. Saleable Unit UPC: 742365004322 (6-8 FL OZ Milk Boxes). Case: ORG MILK 1% DHA CHOCOLATE 3/6PK (item 136518). Case UPC: 742365004322. Three 6-Packs, 18-8Package integrity compromised.
- Class II
Medical Device Recall · March 11, 2026
Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for treatment of atrial flutter.Ventricular fibrillation (VF) occurred during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable Cardioverter Defibrillator (ICD) or Biotronik Cardiac Resynchronization Therapy-Defibrillator (CRT-D) implanted. The observation is caused by an interaction between the Sphere-9 catheter current flow and a safety feature built into Biotronik ICDs and CRT Ds. Medtronic recommends physicians use increased caution when using the Sphere-9 catheter for RF ablation therapy in patients implanted with a Biotronik ICD/CRT-D system, and to ensure external defibrillation systems are readily available.
- Class II
Medical Device Recall · March 11, 2026
MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous AcceDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 1,000 mL in a Single Dose freeflex bag, 1,000 mLx10, Fresenius Medical Care, Waltham, MA 02451, Distributed by: Fresenius Medical CLack of Assurance of Sterility
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, 0.9% (900 mg per 100 mL) (9 mg per mL) 100 mL in a 100 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 600047, Unit of Use NDLack of Assurance of Sterility
- Class II
Drug Recall · March 11, 2026
0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 100 mL in a Single Dose freeflex bag, Rx only, BD Beckton, Dickson and Company, 1 Beckton Drive, Franklin Lakes, NJ 07417 USA, DistLack of Assurance of Sterility
- Class I
Food Recall · March 11, 2026
MILK-N-EGG MIX NET WEIGHT: 50 LBS, PROCESSED FROM NONFAT DRIED MILK, DRIED WHEY, DRIED EGG WHITES CONTAINS: EGG, MILK Mfred By: Griffith Goods, One Griffith Way, Stonecrest, GAPotential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
- Class II
Food Recall · March 11, 2026
TETAS Mireya, Cherry Milkshake (Colita con Leche), i unit Popsicle, Net wt 6OZ. 170GRS. KEEP FROZEN. UPC Code 83822654822Undeclared allergen: Soy Lecithin
- Class II
Medical Device Recall · March 10, 2026
Siemens Medical Solutions USA, Inc
ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing significantly higher, the actual applied x-ray dose levels are in accordance with the system settings and imaging conditions, as well as the applicable regulatory requirements.
- Class II
Medical Device Recall · March 10, 2026
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 USAn internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the actuator's ability to hold the load, leading to rapid and uncontrolled downward movement of the lifting arm.
- Class I
Food Recall · March 10, 2026
Nuts.com, Espresso Malted Milk Balls, 1 lb. sealed pouch & 20 lb. clear poly bag in Nuts.com cardboard box . Packages are only sold individually .Undeclared Allergen - Wheat and Soy (from Soy Lecithin). The ingredient statement and allergen information do not include wheat or soy.
- Class II
Medical Device Recall · March 9, 2026
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717HMedical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
- Class II
Medical Device Recall · March 9, 2026
LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
- Class II
Medical Device Recall · March 9, 2026
LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
- Class II
Medical Device Recall · March 9, 2026
Siemens Medical Solutions USA, Inc
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray systemDuring patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.
- Class II
Medical Device Recall · March 9, 2026
LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.