Safety Recall Directory
Browse and filter the latest official safety alerts globally.
Showing 24 of 74,116 results
Safety Alert
CPSC
CPSCZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
Unknown Firm
CPSCGeneral Alert
ZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
Apr 16, 2026
Safety AlertCPSC
CPSCLe Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Unknown Firm
CPSCGeneral Alert
Le Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
Apr 16, 2026
Medical DeviceFDA Devices
FDA DevicesNAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007; 5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007; 6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.
Medline Industries, LP
FDA DevicesClass I
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007; 5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007; 6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Apr 15, 2026Medline Industries, LP
Food & BeverageFDA Food
FDA FoodBoner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603
Pure Vitamins and Natural Supplements, LLC
FDA FoodClass I
Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603
FDA analysis revealed the presence of undeclared sildenafil and Tadalafil
Apr 15, 2026Pure Vitamins and Natural Supplements, LLC
PharmaceuticalFDA Drugs
FDA Drugs0.9% 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.
Fresenius Kabi USA, LLC
FDA DrugsClass II
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 Sale NDC Number: 65219-466-60.
Lack of Assurance of Sterility
Apr 15, 2026Fresenius Kabi USA, LLC
PharmaceuticalFDA Drugs
FDA DrugsLanreotide 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
Cipla USA, Inc.
FDA DrugsClass II
Lanreotide 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.
Apr 15, 2026Cipla USA, Inc.
PharmaceuticalFDA Drugs
FDA DrugsIsotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2436-15 (carton), NDC 0591-2436-45 (blister pack).
Teva Pharmaceuticals USA, Inc
FDA DrugsClass II
Isotretinoin Capsules, USP, 40 mg, 10 count Prescription Pacs, Rx only, Manufactured for: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0591-2436-15 (carton), NDC 0591-2436-45 (blister pack).
Superpotent and Subpotent
Apr 15, 2026Teva Pharmaceuticals USA, Inc
PharmaceuticalFDA Drugs
FDA Drugs0.9% 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.
Fresenius Kabi USA, LLC
FDA DrugsClass II
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"), Unit of Sale NDC Number: 17271-701-02.
Lack of Assurance of Sterility
Apr 15, 2026Fresenius Kabi USA, LLC
Food & BeverageFDA Food
FDA FoodZarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl oz cups and 32 fl oz cups translucent freezer grade and round High-Density Polyethylene container with lid and 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
Zarlengo Italian Ice
FDA FoodClass II
Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl oz cups and 32 fl oz cups translucent freezer grade and round High-Density Polyethylene container with lid and 1 Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Apr 15, 2026Zarlengo Italian Ice
Food & BeverageFDA Food
FDA FoodFresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrugated cardboard cartons; 6-12 melons per box; individual carton count per label. Keep refrigerated; store between 36 40¿F.
AYCO FARMS INC
FDA FoodClass I
Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped in food safe plastic bags packed in corrugated cardboard cartons; 6-12 melons per box; individual carton count per label. Keep refrigerated; store between 36 40¿F.
Potential Salmonella Contamination
Apr 15, 2026AYCO FARMS INC
Food & BeverageFDA Food
FDA FoodReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz, UPC 8 26766 25036 3. Distributed By F&S Fresh Foods Vineland, NJ 08360. Label declares CONTAINS EGG, MILK, SOY, WHEAT.
F&S Fresh Foods, Inc.
FDA FoodClass II
ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz, UPC 8 26766 25036 3. Distributed By F&S Fresh Foods Vineland, NJ 08360. Label declares CONTAINS EGG, MILK, SOY, WHEAT.
Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.
Apr 15, 2026F&S Fresh Foods, Inc.
PharmaceuticalFDA Drugs
FDA Drugs5% 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: 65219-458-30.
Fresenius Kabi USA, LLC
FDA DrugsClass II
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: 65219-458-30.
Lack of Assurance of Sterility
Apr 15, 2026Fresenius Kabi USA, LLC
PharmaceuticalFDA Drugs
FDA DrugsArtificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg: Geri-Care; Brooklyn, New York NDC 68788-7266-0
Preferred Pharmaceuticals, Inc.
FDA DrugsClass II
Artificial Tears Lubricant Eye Drops (glycerin 0.2%, hypromellose 0.2%, polyethylene glycol 400 1%), 0.5 oz bottles, Mfg: Geri-Care; Brooklyn, New York NDC 68788-7266-0
Lack of Assurance of Sterility
Apr 15, 2026Preferred Pharmaceuticals, Inc.
Medical DeviceFDA Devices
FDA DevicesMedline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B
Medline Industries, LP
FDA DevicesClass I
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Apr 15, 2026Medline Industries, LP
PharmaceuticalFDA Drugs
FDA Drugs0.9% 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.
Fresenius Kabi USA, LLC
FDA DrugsClass II
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: 65219-472-05, Unit of Sale NDC Number: 65219-472-20.
Lack of Assurance of Sterility
Apr 15, 2026Fresenius Kabi USA, LLC
Food & Beverage
Germany BVL
Germany BVLSAMYANG Instant Nudeln Scharfes Huhn Carbonara Cup 6 x 80 Gramm
Heuschen & Schrouff Oriental Foods Trading B.V., Sperwerweg 1, 6374 AG Landgraaf
Germany BVLGeneral Alert
SAMYANG Instant Nudeln Scharfes Huhn Carbonara Cup 6 x 80 Gramm
Rückstände und Kontaminanten
Apr 15, 2026Heuschen & Schrouff Oriental Foods Trading B.V., Sperwerweg 1, 6374 AG Landgraaf
Food & BeverageGermany BVL
Germany BVLGutmann Alkoholfreies Hefeweizen, 0,5 Liter, zwei Sorten
Brauerei Gutmann e.K., Titting
Germany BVLGeneral Alert
Gutmann Alkoholfreies Hefeweizen, 0,5 Liter, zwei Sorten
Sonstige Gründe
Apr 15, 2026Brauerei Gutmann e.K., Titting
Pharmaceutical
Australia
AustraliaArtri Ajo King tablets
TGA
au-tgaMedicines Safet...
Artri Ajo King tablets
We are advising consumers that Artri Ajo King tablets may pose a serious risk to your health and should not be taken....
Apr 15, 2026TGA
Food & BeverageFDA Food
FDA FoodCrab Cakes various sizes sold to food service
Connecticut Crab Company LLC
FDA FoodClass II
Crab Cakes various sizes sold to food service
May be temperature abused, which may result in growth of Clostridium botulinum
Apr 15, 2026Connecticut Crab Company LLC
Vehicle RecallNHTSA
NHTSAVolkswagen Group of America, Inc. - Brake Pedal May Detach from Brake Booster
Volkswagen Group of America, Inc.
NHTSASERVICE BRAKES,...
Volkswagen Group of America, Inc. - Brake Pedal May Detach from Brake Booster
Brake pedal detachment can cause a loss of brake function and increase the risk of a crash.
Apr 15, 2026Volkswagen Group of America, Inc.
Medical DeviceFDA Devices
FDA DevicesMedline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596
Medline Industries, LP
FDA DevicesClass I
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Apr 15, 2026Medline Industries, LP
Medical DeviceFDA Devices
FDA DevicesTornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max Tuberosity Body No Coat, Small, Cat. No. ARS1041102 3. TORNIER HRS Max Trial, Cat. No. ARS10252
Tornier, Inc
FDA DevicesClass II
Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max Tuberosity Body No Coat, Small, Cat. No. ARS1041102 3. TORNIER HRS Max Trial, Cat. No. ARS10252
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.
Apr 15, 2026Tornier, Inc
Medical DeviceFDA Devices
FDA DevicesSee Luer Cap Set, MPC-130, set, administration, intravascular
Molded Products Inc
FDA DevicesClass II
See Luer Cap Set, MPC-130, set, administration, intravascular
Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.
Apr 15, 2026Molded Products Inc
Medical DeviceFDA Devices
FDA DevicesMicroScan Neg MIC 3J REF C54814
Beckman Coulter, Inc.
FDA DevicesClass II
MicroScan Neg MIC 3J REF C54814
Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
Apr 15, 2026Beckman Coulter, Inc.