All recalls
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II5% 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: 65219-456-60.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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, Distributed by BD, Manufactured by Fresenius Kabi, Unit of Sale NDC Number: 17271-701-07.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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 Care RTG, LLC, Manufactured by: Fresenius Kabi, Unit of Use NDC: 65219-282-01, Unit of Sale NDC Number: 65219-282-10.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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 Use NDC: 65219-432-20, Unit of Sale NDC Number: 65219-432-85.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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, Distributed by BD, Manufactured by: Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Sale NDC Number: 17271-701-05.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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, Distributed by BD, Manufactured by: Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Sale NDC Number: 17271-701-03.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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"), Unit of Sale NDC Number: 17271-701-02.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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: 65219-472-05, Unit of Sale NDC Number: 65219-472-20.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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: 65219-470-05, Unit of Sale NDC Number: 65219-470-30.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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 NDC: 65219-468-05, Unit of Sale NDC Number: 65219-468-50.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.9% 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 Sale NDC Number: 65219-466-60.
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugFresenius Kabi USA, LLCClass II0.45% 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 NDC: 63323-626-03, Unit of Sale NDC Number: 63323-626-25 (30 bags in 1 case).
Lack of Assurance of Sterility
- 2026-04-15FDA-DrugCipla USA, Inc.Class IILanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only, Rx Only, Manufactured by: Pharmathen International, S.A., Rodopi, Greece. Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC 69097-906-67
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
- 2026-04-15FDA-DrugCipla USA, Inc.Class IILanreotide Injection, 120 mg*/0.5 mL, Box contains 1 Pre-filled syringe and 1 safety needle, Single dose only, Rx Only, Manufactured by: Pharmathen International, S.A., Rodopi, Greece. Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
- 2026-04-09FDA-PRProduct Recall
Nail Polish Remover recalled due to the detection of methylene chloride and chloroform in the affected product—both hazardous substances that are strictly prohibited in cosmetic formulations.
- 2026-04-09USDAPublic Health AlertFSIS Issues Public Health Alert for Beef and Pork Products Due to Misbranding and Undeclared Allergen
Misbranding, Unreported Allergens
- 2026-04-09NHTSA-EquipmentWeldon Division of Akron BrassWeldon Division of Akron Brass — Touch Screen Display May Fail
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.
- 2026-04-09NHTSA-EquipmentNova Bus (US) Inc.Nova Bus (US) Inc. — Window Glass May Detach from Frame/FMVSS 217
The glass can fall out of the frame, increasing the risk of ejection and injury during a crash. Detached window glass can also become a road hazard for other vehicles, increasing the risk of a crash.
- 2026-04-09CPSCQingyuan Fenle Sauna & Pool Equipment Co., Ltd., of ChinaMuscccm Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by SZ Hengxun
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.
- 2026-04-09CPSCPrestige Import Group, of Deerfield, FloridaPrestige Import Group Recalls Supernova and Typhoon Lighters Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Cigarette Lighters
The recalled lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanism, posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.
- 2026-04-09CPSCJ U Kai Technology Co., LTD, dba Happiness Light, of ChinaLED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries; Sold on Amazon by Happiness Light
The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-04-09CPSCShenzhen Shijingjie Network Technology Co., Ltd., of ChinaShenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled Due to Risk of Serious Injury and Death from Electrocution and Carbon Monoxide Poisoning Hazards; Sold on Walmart
The recalled male-to-male extension cords violate safety requirements because their exposed prongs can become energized when one end is plugged into a generator or other power source, posing a risk of serious injury and death from electrocution. In addition, using the cords to supply power from a generator to a residential electrical system (backfeeding) poses a risk of electrocution and fire. The cords' short length encourages the use of generators close to homes or enclosed spaces, posing a risk of carbon monoxide (CO) poisoning.
- 2026-04-09CPSCShenzhen Baihang Technology Co., Ltd., of ChinaShenzhen Baihang Recalls VEEKTOMX Mini Power Banks, Due to Fire and Burn Hazards; Sold on Amazon
The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.
- 2026-04-09CPSCShymeryDirect, of ChinaShymeryDirect LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. If coin batteries are swallowed, they can cause serious injuries, internal chemical burns and death.
- 2026-04-09CPSCWeifang Luzhan Trade Co., Ltd., dba Yeeluzan, of ChinaYeeluzan Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Yeeluzan
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.
- 2026-04-09CPSCLinkInnow International Co., Ltd., dba Besslly Store, of ChinaHalloween Pumpkin Carving Kits Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Besslly Store
The recalled carving kits violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries in the tea lights can be accessed easily by children, posing an ingestion hazard. Additionally, the product and its packaging do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.
- 2026-04-09CPSCHead USA Inc., of Boulder, ColoradoHead USA Recalls Ski Boots Due to Risk of Serious Injury from Fall Hazard
The fluorescent yellow materials of the boot shell and sole inserts can deteriorate and break, posing a risk of serious injury from a fall.
- 2026-04-09CPSCSeasonal Specialties, LLC, of Eden Prairie, MinnesotaSeasonal Specialties Recalls Members Mark 7' Pre-Lit Twinkling Bucks Due to Burn Hazard
If the wires are connected incorrectly, the current limiting resistor can overheat, posing a burn hazard.
- 2026-04-09CPSCJohnson Outdoors Diving LLC d/b/a SCUBAPRO, of Racine, WisconsinSCUBAPRO Recalls Monorail Weight Pockets for Buoyancy Compensator Devices (BCDs) Due to Risk of Serious Injury or Death from Drowning
The D-ring handle that is used to unlock the weight pocket from the Buoyancy Compensator Device (BCD) can detach during use. If this happens, the user will not be able to remove the weight pocket in an emergency, in order to rise to the surface, posing a risk of serious injury or death from a drowning hazard.
- 2026-04-09CPSCHefei Maitusilu Wangluokeji Youxiangongsi, dba Maitys, of ChinaMagnetic Drinkware Charms Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets; Sold on Amazon by Maitys
The recalled magnetic drinkware charms violate the mandatory standard for magnets because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.