Safety Recalls

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

Showing 1,101–1,150 of 15,182

• Medical Device Recall · April 14, 2026

  Philips North America

  Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148. 3. Model Number (REF): 782166.

  The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

  Class II

• Medical Device Recall · April 14, 2026

  Dexcom, Inc.

  Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: Versions 2.9.0 through 2.11.2 Product Description

  A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then "replay" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.

  Class II

• Food Recall · April 14, 2026

  LACTALIS CANADA, INC

  Specially SELECTED brand Vanilla Creme Brulee; NET WT 3.6oz (103g); INGREDIENTS: CREAM (MILK, CREAM), FROZEN YOLK MIX (EGG YOLK, SUGAR) SUGAR, NATURAL VANILLA FLAVOR, TAPIOCA STARCH, CARRAGEENAN; TOPP

  Product may contain foreign objects, specifically glass.

  Class II

• Medical Device Recall · April 13, 2026

  Physio-Control, Inc.

  LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 9

  Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.

  Class II

• Drug Recall · April 13, 2026

  Unichem Pharmaceuticals USA Inc.

  busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind, Area, Meerut Road, Ghazibad - 201 003, India Manufactured for: Unichem Pharmaceut

  Subpotent drug

  Class III

• Medical Device Recall · April 13, 2026

  HF Acquisition Co LLC

  Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Descriptio

  Due to incorrect incubation process being performed on product.

  Class II

• Food Recall · April 13, 2026

  Raja Foods and Vegetables Inc.

  Swad Orange Flavored Masala Candy

  Contains undeclared FD&C Yellow 6

  Class II

• Medical Device Recall · April 13, 2026

  O&M HALYARD INC

  Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)

  Nitrile Exam Glove failed to meet specifications chemical permeation performance.

  Class II

• Medical Device Recall · April 13, 2026

  HF Acquisition Co LLC

  Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Descriptio

  Due to incorrect incubation process being performed on product.

  Class II

• Food Recall · April 13, 2026

  Guangdong Zonegoing Food Co., LTD

  52USA brand POPPING BOBA; PASSION FRUIT FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-m

  Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

  Class II

• Medical Device Recall · April 13, 2026

  Jolife AB

  LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875

  Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the passing results were not include in the service records).

  Class II

• Food Recall · April 13, 2026

  Guangdong Zonegoing Food Co., LTD

  52USA brand POPPING BOBA; STRAWBERRY FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-mali

  Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

  Class II

• Food Recall · April 13, 2026

  Guangdong Zonegoing Food Co., LTD

  52USA brand POPPING BOBA; MANGO FLAVOR; Net wt: 7 lb (3.2kg); Ingredients Drinking water, fructose syrup, food additives (hydroxypropyl distarch phosphate (E1442), calcium lactate (E327), DL-malic aci

  Products contain unapproved colors, specifically tartrazine (FD&C Yellow 5), sunset yellow (FD&C Yellow 6), and allura red (FD&C Red 40).

  Class II

• Food Recall · April 13, 2026

  Raja Foods and Vegetables Inc.

  Swad Mango Flavored Masala Candy

  Contains undeclared Blue 1

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJ

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Integra LifeSciences Corp. (NeuroSciences)

  Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diver

  Out-of-specification endotoxin result that did not meet the acceptance criteria.

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU DYNJRA1555; 2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817;

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B;

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  ARROW INTERNATIONAL, LLC

  Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15192-VFI, CS-15192-VFIE, CS-15232-VFI, CS-15232-VFIE, CS-15272-VFI, CS-15272-VFIE,

  16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

  Class I

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  ARROW INTERNATIONAL, LLC

  NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272-SFX, CS-15312-SFX, CS-15422-SFX, CS-15502-SFX; NextStep Antegrade Hemodialy

  16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P

  Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister pack are labeled as a 1 mL Luer Lock Tuberculin Syringe (Product Code 1180100777), but the syringes inside are U-100 insulin syringes.

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD Dynamic Tip Steerable, Product Number 6DYNTP001;

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A; 2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  ARROW INTERNATIONAL, LLC

  Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, CS-15552-VSP, CSD-15242-SP, CSD-15282-SP; Cannon II Plus Hemodialysis Catheter with Arrow Simplici

  16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II