Safety Recalls
RSS ↗17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 1,701–1,750 of 17,553
- Class III
Food Recall · May 19, 2026
ESTRELLA, Bebida de Parcha (Passion Fruit Drink), multiple sizes, 14 OZ.FL. (413 ML), 64 OZ.FL (1,920mL), 120 OZ.FL. (3.54LT.) 14 OZ.FL Plastic Bottles packed in cases of 25 bottles. KEEP REFRIGIRATEUndeclared FD&C Red 40
- Class II
- Class II
Medical Device Recall · May 19, 2026
Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit) ACEN89-02; 3) BACK PACK, Model/Item Number (kit) ALBK51-01; 4) DR DERIAThe recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
- Class I
Food Recall · May 19, 2026
Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ (1 Lb 8OZ) 680g. Case Label: Whole Foods Global Minestrone Soup 702505, KEEP REContains undeclared allergen (shrimp).
- Class II
Medical Device Recall · May 18, 2026
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)Sterile wound dressing, lacks sterility assurance
- Class I
Food Recall · May 18, 2026
Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly BagsUndeclared Tree Nut Allergen
- Class II
Medical Device Recall · May 18, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Detector; Model # 708036 for MultiDiagnost EPhilips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
- Class II
Medical Device Recall · May 18, 2026
ProNephro AKI (NGAL) Reagent Kit (100 tests). IVD Acute Kidney Injury Test System.The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring of renal disease in intended users.
- Class II
Medical Device Recall · May 18, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xper FD10F; Model # 722003 for Allura Xper FD10; Model # 722005 for Allura Xper FDPhilips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection
- Class III
Drug Recall · May 18, 2026
Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520. NDC: 55150-164-02Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
- Class II
Food Recall · May 18, 2026
International Food Products Corporation
Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bagsPotential for Salmonella
- Class III
Drug Recall · May 18, 2026
PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicago, IL 60064, Product of France, NDC 11980-174-10.Failed Stability Specifications
- Class II
Medical Device Recall · May 18, 2026
GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.
- Unclassified
Vehicle Recall · May 18, 2026
2026 KEYSTONE MONTANALoose shock bolts may cause a loss of vehicle stability, increasing the risk of a crash.
- Class II
Food Recall · May 18, 2026
International Food Products Corporation
Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bagsProduct tested positive for Salmonella
- Class I
Medical Device Recall · May 18, 2026
Impella CP Set with SmartAssist. Product Codes: 1000080, 1000851, 0048-0014, 0048-0024-JP.Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.
- Class II
Food Recall · May 18, 2026
International Food Products Corporation
Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb boxPotential for Salmonella
- Class II
Drug Recall · May 18, 2026
PReye Vitamin See Antioxidant Preservative Free Eye Drops, Distributed by: PReye, LLC, Golden, COLack of Assurance of Sterility
- Class II
Food Recall · May 15, 2026
U.S. Tov, Inc. dba U.S. Trading Company
DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward, CA 94545-1130 UPC: 721557533567Potential contamination with lead.
- Class II
Medical Device Recall · May 15, 2026
ALYON Surgical Lighting SystemThe the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- Class II
Food Recall · May 15, 2026
Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated case of 18 packages (4.5oz net wt.) individually wrapped in laminated film. This prFirm observed oily and sticky substance on direct food contact surface packaging of finished product.
- Class I
Medical Device Recall · May 15, 2026
Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude MedExpansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge during use and contact circulating blood or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
- Class II
Medical Device Recall · May 15, 2026
HarmonyAIR A-Series Surgical Lighting SystemThe the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- Class II
Medical Device Recall · May 15, 2026
HarmonyAIR A-Series Surgical Lighting SystemThere is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
- Unclassified
Vehicle Recall · May 15, 2026
2025 HYUNDAI ELANTRA HYBRIDOverheating in the HPCU increases the risk of a fire.
- Class II
Drug Recall · May 15, 2026
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-04.Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- Class II
Food Recall · May 15, 2026
Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry conditions .Foreign material (Glass) was found in the product.
- Class II
Drug Recall · May 15, 2026
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- Class II
Drug Recall · May 15, 2026
VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-2Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- Class II
Drug Recall · May 15, 2026
VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in 240 mL (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-2Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- Class I
Food Recall · May 14, 2026
Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
- Class I
Medical Device Recall · May 14, 2026
Automated Impella Controller (AIC), for use with left heart support blood pump. Labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioxiPotential for overpressure alerts.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS12-120LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioPotential for overpressure alerts.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-75LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioxidePotential for overpressure alerts.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for LapaPotential for overpressure alerts.
- Class III
Drug Recall · May 14, 2026
Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696-02 (vial), NDC 63323-696-25 (carton)Failed Impurities/Degradations Specifications
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioxidPotential for overpressure alerts.
- Unclassified
Vehicle Recall · May 14, 2026
2025 CADILLAC ESCALADE, 2025 CADILLAC ESCALADE ESV, 2025 CHEVROLET TAHOE, 2025 GMC YUKON, 2025 GMC YUKON XLA bolt that loosens or breaks during vehicle operation can result in loss of vehicle control, increasing the risk of a crash.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS8-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioxidPotential for overpressure alerts.
- Unclassified
Consumer Product Recall · May 14, 2026
Shenzhen Jiangtou Technology Co., Ltd., dba Remy&shop
Superbobi 7 3/8 Inch Pool Drain CoversThe 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.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator forPotential for overpressure alerts.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioxidPotential for overpressure alerts.
- Class II
Medical Device Recall · May 14, 2026
ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon DioxiPotential for overpressure alerts.
- Unclassified
Consumer Product Recall · May 14, 2026
Amazon.com Services LLC, of Seattle, Washington
Amazon Basics 55 Lbs. Adjustable DumbbellsThe weight plates can fail to engage completely during weight adjustment and dislodge from the dumbbell handle when used, posing an impact hazard.
- Unclassified
Consumer Product Recall · May 14, 2026
Petzl America, Inc., Salt Lake City, Utah
Petzl SIMBA CLIMBING and SIMBA PARK Children's Harnesses, SWAN EASYFIT STEEL and SWAN EASYFIT STAINLESS HarnessesThe recalled harnesses are missing rivets in the FAST LT PIN-LOCK buckles, causing the buckles to open, posing a risk of serious injury or death from a fall hazard.
- Unclassified
Consumer Product Recall · May 14, 2026
SuzhouGongYeYuanQu Wan Yi Shen Jia MaoYiShangHang dba Cosyland Official, of China
Cosyland Children's Tower StoolsThe recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.
- Unclassified
Consumer Product Recall · May 14, 2026
Petzl America, Inc., Salt Lake City, Utah
Petzl ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnessesThe recalled harness' D-ring can release, allowing the attachment point to open, posing a risk of serious injury or death from a fall hazard.