Safety Recalls

15,182 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,251–1,300 of 15,182

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Cake de Coco [image] Coconut Cake The Original, Net Wt. 47 oz, packaged in a rigid plastic clamshell container with a transparent dome lid and tray base, one unit per container. KEEP REFRIGERATED. UPC

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Tiramisu [image] Cofee Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790850320

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Cheesecake de Mango [image] Mango Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852836

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Jumbo Brazo Gitano Caramelo [image] Jumbo Caramel Roll The Original, Net Wt. 40 oz, packaged in a rigid plastic clamshell container with a transparent dome lid, one unit per container. KEEP REFRIGERAT

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Food Recall · April 3, 2026

  Walker Honey Co

  Dark Pecan Creamed Honey/Pecan Creamed Honey 671333101407 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Cre

  Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

  Class II

• Food Recall · April 3, 2026

  Walker Honey Co

  Cinnamon Creamed Honey 671333101360 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Wh

  Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

  Class II

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Marquesita de Dulceleche [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 8

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Food Recall · April 3, 2026

  Walker Honey Co

  Natural Creamed Honey, 671333101377 *These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whi

  Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

  Class II

• Food Recall · April 3, 2026

  Walker Honey Co

  Blackberry Creamed Honey 671333101308 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz

  Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

  Class II

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Flan Cake [image] Custard Cake The Original, Net Wt. 30 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852959

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Food Recall · April 3, 2026

  Galaxy RG Corp

  Napolitano [image] Neapolitan The Original, Net Wt. 22 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852256

  Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

  Class II

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  One Step K in vitro diagnostic test REF: 81A4

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Medical Device Recall · April 2, 2026

  Merit Medical Systems, Inc.

  Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY

  catheter may experience resistance when being advanced over the guidewire

  Class II

• Medical Device Recall · April 2, 2026

  Cook Incorporated

  Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials a

  Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

  Class I

• Drug Recall · April 2, 2026

  B BRAUN MEDICAL INC

  0.9 % SODIUM CHLORIDE IRRIGATION, USP, 3000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7388-60.

  Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

  Class II

• Medical Device Recall · April 2, 2026

  Merit Medical Systems, Inc.

  Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY

  catheter may experience resistance when being advanced over the guidewire

  Class II

• Food Recall · April 2, 2026

  Raw Farm LLC

  RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP REFRIGERATED INGREDIENTS: WHOLE RAW MILK, VEGETABLE RENNET, CULTURES, K

  Multi-state outbreak of E. coli O157:H7.

  Class I

• Consumer Product Recall · April 2, 2026

  OCUN NA LLC, of Park City, Utah

  Ocun Condor HMS Triple Locking Carabiners

  The carabiner's gate can malfunction where the gate does not close automatically and has to be closed manually by hand, posing a risk of serious injury or death due to falling.

  Unclassified

• Consumer Product Recall · April 2, 2026

  Dongguan Oukatuo Electronic Technology Co., Ltd., dba BUDI Official, of China

  Coluans Christmas Light-Up Rings Party Favors

  The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · April 2, 2026

  Zhongshan KDB Health Solutions Co., Ltd., of China

  Sangohe Adult Portable Bed Rails

  The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required warning labels.

  Unclassified

• Vehicle Recall · April 2, 2026

  Ember Recreational Vehicles, INC

  2026 EMBER E-SERIES

  Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.

  Unclassified

• Drug Recall · April 2, 2026

  Huons Co., Ltd.

  Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP (15 mg/2 mL) (7.5 mg/mL) ampules, Rx only, Manufactured by: Houns Co., Ltd, 100, Bio valley, Je-cheor-Si, Chungcheongbuk-dc, Korea, NDC

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · April 2, 2026

  Cook Incorporated

  Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 NR5.0-35-100-P-10S-0-CSC-20 G31214 NR5.0-35-100-P-10S-PIG-CSC-20 G31216 NR5.0-35-70-P-10S-VCF-CSC-20 G31220 NR

  Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

  Class I

• Food Recall · April 2, 2026

  Raw Farm LLC

  RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt, 100%

  Multi-state outbreak of E. coli O157:H7.

  Class I

• Food Recall · April 2, 2026

  Raw Farm LLC

  RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160

  Multi-state outbreak of E. coli O157:H7.

  Class I

• Medical Device Recall · April 2, 2026

  Intuitive Surgical, Inc.

  Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4200 Software Version: N/A Product Description: he da Vinci Xi, X Surgical syst

  Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.

  Class II

• Consumer Product Recall · April 2, 2026

  Huizhou Haitan Technology Co., Ltd., of China

  HTRC and Haisito battery chargers

  The chargers can ignite or cause a connected battery to ignite, posing a fire hazard and risk of serious injury and death.

  Unclassified

• Consumer Product Recall · April 2, 2026

  Samson International, of High Point, North Carolina

  Universal Broadmoore brand Bellevue and Oaklynn model canopy bed frames

  The canopy beams of the bed frames can collapse primarily when the bed is moved, posing impact and injury hazards to consumers.

  Unclassified

• Medical Device Recall · April 2, 2026

  Windstone Medical Packaging, Inc.

  Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA Syringes) Angio Pack Part numbers AMS6908E, AMS6908F

  Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.

  Class I

• Drug Recall · April 2, 2026

  B BRAUN MEDICAL INC

  DEXTROSE INJECTION USP, 70%, 2000 mL bags, Rx only, Sterile, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7387-50.

  Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

  Class II

• Vehicle Recall · April 2, 2026

  FONTAINE MODIFICATION CO.

  2025 FREIGHTLINER BUSINESS CLASS M2

  A lack of lubrication may cause binding gears and difficulty steering, increasing the risk of a crash.

  Unclassified

• Drug Recall · April 2, 2026

  B BRAUN MEDICAL INC

  LACTATED RINGER'S IRRIGATION, 3000 mL bags, Sterile, Ex only, B. Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC: 0264-7389-60.

  Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

  Class II

• Drug Recall · April 2, 2026

  B BRAUN MEDICAL INC

  Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 18018-3524, NDC: 0264-7385-60.

  Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.

  Class II

• Food Recall · April 2, 2026

  Wawa Beverage Company

  Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle

  Undeclared Milk Allergen,

  Class I

• Drug Recall · April 2, 2026

  Huons Co., Ltd.

  Lidocaine HCl injection, USP, 1% 50mg/5mL (10 mg/mL), 5 mL Single Dose Vials, Rx only, Manufactured by: Huons Co, Ltd, Chungcheongbuk-do, Korea NDC 73293-0001-1 (vial), NDC 73293-0001-2 (10 count cart

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  One Step UTI in vitro diagnostic test REF: 3374

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  QUCARE Total Cholesterol in vitro diagnostic test REF: 6407

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Drug Recall · April 2, 2026

  Huons Co., Ltd.

  0.9% Sodium Chloride Injection, USP, 10 mL Ampules, Rx only, Single Dose, Preservative Free, Manufactured for: Spectra Medical Devices, LLC, Wilmington, MA, 01887, By: Houns Co., Ltd, Jecheon, Korea,

  Lack of Assurance of Sterility

  Class II

• Drug Recall · April 2, 2026

  Huons Co., Ltd.

  Lidocaine HCl Injection, USP, 2%, 100 mg/5mL (20 mg/mL), 5 mL Single-Dose Vials, Rx only, Manufactured by: Huons Co., Ltd., 100 Bio valley-ro, Jecheon-si, Chungchengbuk-do, Korea, NDC 73293-0003-1 (vi

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · April 2, 2026

  Cook Incorporated

  Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiogra

  Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

  Class I

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  One Step pH in vitro diagnostic test REF: 31I4P

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Medical Device Recall · April 2, 2026

  Merit Medical Systems, Inc.

  Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY

  catheter may experience resistance when being advanced over the guidewire

  Class II

• Food Recall · April 2, 2026

  Wawa Beverage Company

  Wawa Diet Lemonade Pint (16oz), Plastic bottle

  Undeclared Milk Allergen,

  Class I

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  One Step 10A in vitro diagnostic test

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Medical Device Recall · April 2, 2026

  Siemens Healthcare Diagnostics Inc

  epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;

  Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous, and capillary patient samples. An erroneously low pH or mTCO2 reading can lead to inappropriate treatment of nonexistent acidosis (respiratory of metabolic) or missed diagnosis of alkalosis (a true high pH: respiratory or metabolic alkalosis), potentially causing harm through unnecessary interventions with the former or failure to deliver appropriate treatment with the latter.

  Class II

• Consumer Product Recall · April 2, 2026

  Dongguan Qicaifeng Trading Co., Ltd., dba Beestech, of China

  Beestech Children's Spiral Tower Toys

  The recalled spiral tower toy sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

  Unclassified

• Food Recall · April 2, 2026

  Wawa Beverage Company

  Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle

  Undeclared Milk Allergen,

  Class I

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  Uric Acid in vitro diagnostic test REF: 31H0P

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Food Recall · April 2, 2026

  Raw Farm LLC

  RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt Produc

  Multi-state outbreak of E. coli O157:H7.

  Class I

• Food Recall · April 2, 2026

  Wawa Beverage Company

  Wawa Fruit Punch Pint (16oz), Plastic bottle

  Undeclared Milk Allergen,

  Class I