Safety Recalls

15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 2,251–2,300 of 15,186

• Drug Recall · January 26, 2026

  F.H. INVESTMENTS, Inc. (dba Asteria Health)

  Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32

  Presence of Foreign substance - potential presence of metal particulate matter

  Class II

• Drug Recall · January 26, 2026

  F.H. INVESTMENTS, Inc. (dba Asteria Health)

  Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4079-32.

  Presence of Foreign substance - potential presence of metal particulate matter

  Class II

• Drug Recall · January 26, 2026

  F.H. INVESTMENTS, Inc. (dba Asteria Health)

  ESTRADIOL, 6 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3006-32.

  Presence of Foreign substance - potential presence of metal particulate matter

  Class II

• Food Recall · January 26, 2026

  Beacon Promotions Inc

  Repackaged M&Ms Peanut candies, Net Wt 1.3 oz. Item BB471BG. Labeled as Make Your Mark. For nutrition facts information and ingredients, go to https://hpgbrands.com/sugarspot-nutrition/

  Undeclared allergens (milk, soy, and peanut)

  Class II

• Medical Device Recall · January 26, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X

  Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

  Class II

• Food Recall · January 26, 2026

  Gerber Products Company dba Nestle Infant Nutrition

  Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015000005962, packed 4 bags/case with UPC 015000935726; Made for Gerber Products Co., Fremont, MI 49413

  Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.

  Class II

• Medical Device Recall · January 26, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

  Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

  Class II

• Drug Recall · January 26, 2026

  F.H. INVESTMENTS, Inc. (dba Asteria Health)

  Testosterone, 100 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC:79559-1100-32.

  Presence of Foreign substance - potential presence of metal particulate matter

  Class II

• Medical Device Recall · January 26, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X

  Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

  Class II

• Medical Device Recall · January 26, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X

  Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

  Class II

• Medical Device Recall · January 26, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X

  Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

  Class II

• Food Recall · January 24, 2026

  Mangalm LLC

  Tops GOLD Lime Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611397 INGREDIENTS:***Mustard Oil***

  Potential adulteration with erucic acid from mustard oil ingredient.

  Class II

• Food Recall · January 24, 2026

  Mangalm LLC

  Tops GOLD Mango Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611373 INGREDIENTS:***Mustard Oil*** Tops GOLD Mango Pickle NET QTY.: 158.73oz PRODUCT OF INDIA UPC: 8904288611915; 8904288613025

  Potential adulteration with erucic acid from mustard oil ingredient.

  Class II

• Food Recall · January 24, 2026

  Mangalm LLC

  Tops GOLD Khatta Meetha Pickle NET QTY.: 33.51oz PRODUCT OF INDIA UPC: 8904288611427 INGREDIENTS:***Mustard Oil***

  Potential adulteration with erucic acid from mustard oil ingredient.

  Class II

• Food Recall · January 24, 2026

  Mangalm LLC

  Tops GOLD Stuffed Red Chilli Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611953 INGREDIENTS:***Mustard Oil***

  Potential adulteration with erucic acid from mustard oil ingredient.

  Class II

• Food Recall · January 24, 2026

  Mangalm LLC

  Tops GOLD Green Chilli Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288612837 INGREDIENTS:***Mustard Oil***

  Potential adulteration with erucic acid from mustard oil ingredient.

  Class II

• Food Recall · January 24, 2026

  Mangalm LLC

  Tops GOLD Mixed Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611380 INGREDIENTS:***Mustard Oil*** Tops GOLD Mixed Pickle NET QTY.: 158.73oz PRODUCT OF INDIA UPC: 8904288612950 INGREDIENTS:**

  Potential adulteration with erucic acid from mustard oil ingredient.

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with the below descriptions and corresponding article numbers. 1. FLS - Foot Locking Plates System, Cancellous Stabilizati

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article numbers. 1. Forearm Plate, Curved; Article Numbers: 21604-6, 21604-9. 2. Forearm Plate, Strai

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers. 1. Cortical Screw, Locking; Article Numbers: 37351-10-N, 37351-12-N, 37351-14-N, 37351-1

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers. 1. Cortical Screw; Article Numbers: 32151-6, 32151-8, 32151-9, 32151-10, 32151-11, 32151-12, 32151-1

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  I.T.S. Screw System with the below descriptions and corresponding article numbers. 1. Cancellous Screw, Cannulated; Article Numbers: 31404-16, 31404-18, 31404-20, 31404-22, 31404-24, 31404-26, 314

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Brand Name: I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix) with the below descriptions and corresponding article numbers. 1. Anterior Column Plate; Article Numbers: 21218-16, 21219-16.

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10. 2. Clavicle

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Food Recall · January 23, 2026

  Navitas, LLC.

  NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA). Product of Mexico/Argentina/Paraguay. Distributed by Navitas Organics Novato, C

  Potential contamination with Salmonella.

  Class I

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and corresponding article numbers. 1. I.T.S. DUL (Distal Ulna Locking) System, Distal Ulna

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers. 1. Fixation Screw; Article Number: 70312. 2. Spike short; Article Number: 70314.

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated; Article Numbers: 31207-10, 31207-12, 31207-14, 31207-16, 31207-18, 31207-20, 31207-24, 31207-26, 31207-28, 31207-30, 31

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Olecranonplate with Angular Stability with the below descriptions and corresponding article numbers. 1. Olecranon Hook Plate; Article Numbers: 21112-7, 21114-5, 21113-9. 2. Olecranon Plate; Arti

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers. 1. Anterolateral Tibia Plate; Article Numbers: 21311-11, 21311-15, 21311-7, 21312-11, 21312-15, 21

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  Datascope Corp.

  CS100 IABP. Software Version CS100 IABP Q.01.

  The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corresponding article numbers. 1. DFL (Distal Femur Locking) Distal Femur Plate; Article Numbers: 21301-5, 21301-7, 21301

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  Datascope Corp.

  CS300 IABP. Software Version CS300 IABP C.01.

  The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers. 1. Distal Tubular Plate; Article Numbers: 21602-3, 21602-4, 21602-5, 21602-6, 2160

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Medical Device Recall · January 23, 2026

  I.T.S. GmbH

  Brand Name: Humeral Head Plate with Angular Stability, with the following description: Proximal Humeral Plate. Article Numbers: 211341-10, 211341-4, 211341-7, 21134-4, 21134-5, 21135-4, 21136-4, 21136

  Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).

  Class II

• Consumer Product Recall · January 22, 2026

  Brandworl Management Co., Limited, dba Brandworl.USA, of Hong Kong

  Gagaku Wooden Ice Cream Shop Toy Playsets

  The recalled toys violate the mandatory standard for toys because they contain high-powered magnets which can loosen and detach, 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.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Xiaofei He, dba Based Online, of China

  Based Online Fidget Magnet Ball Toys

  The magnet ball toys violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they 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.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Shanghai Zhidi Network Technology Co., Ltd., dba Vndueey, of China

  Vndueey Magnetic Men Toy Sets

  The recalled magnetic stick figure toy sets violate the mandatory standard for toys because the sets contain loose magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they 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.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Thrasio, LLC, of Boston, Massachusetts

  Angry Orange Enzyme Stain Removers

  The recalled products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems, external medical devices, or underlying lung conditions who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by bacteria.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Ningbo Resoul Digital Technology Co., Ltd., of China

  Mikario Trading 5-in-1 Convertible Baby Gyms

  The recalled baby gyms violate the mandatory safety standard for infant support cushions because the floor mats can obstruct an infant's breathing, posing a serious risk of injury or deadly suffocation hazard.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Aborder Products of Irving, Texas

  Cumbor Retractable Safety Gates

  The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment.

  Unclassified

• Food Recall · January 22, 2026

  Lee's Commissary

  Brand: Red Button Movie House Popcorn Pack Size: 24 oz. / 680g. SKU/UPC:4117281332 Shelf life: 150 days. Packaging: Plastic bag Production location: Lee s Commissary 888 W 1600 S Unit 130, Logan Ut. 8

  Product may contain foreign material.

  Class II

• Consumer Product Recall · January 22, 2026

  Xinyude Shenzhen Keji Youxiangongsi, dba Xiyude, of China

  Topkay Torch Lighters

  The recalled lighters violate the mandatory standard for multipurpose lighters because they do not have the required child-resistant mechanisms, posing a risk of serious injury or death from fire and burn hazards.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Academy Ltd., dba Academy Sports + Outdoors, of Katy, Texas

  Magellan Odyssey Rocker Chairs

  The recalled chairs' legs can break, posing injury and fall hazards to consumers.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China

  Iristar Minoxidil Spray Bottles

  The recalled spray bottles contain minoxidil, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Johnson Health Tech Trading, Inc., of Cottage Grove, Wisconsin

  Matrix Retail T30, TF30, T50, TF50, and T75 treadmills, Vision T9800, TF20, T40, and T80 treadmills

  The power cord can become loose from the treadmill's power socket, posing a fire hazard.

  Unclassified

• Consumer Product Recall · January 22, 2026

  Longyan Xinluo District Guiheng E-Commerce Co. Ltd., dba Longyanguiheng, of China

  Yetonamr Pull String Teething Toys

  The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress, serious choking hazard and death.

  Unclassified

• Medical Device Recall · January 21, 2026

  Agiliti Health - Ellis

  Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware

  Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate Management function after using the Autofirm function for 10 minutes. This issue only occurs when the 10-minute timer is allowed to elapse after the Autofirm button is pressed after initial setup, and it only affects the Microclimate Management function.

  Class II