Safety Recalls
RSS ↗15,182 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 1,351–1,400 of 15,182
- Class II
Food Recall · March 26, 2026
Alain MILLIAT; MARMELADE ORANGE; 300 g 10.6 oz; packaged in glass jarsProduct may contain foreign objects, specifically glass.
- Class II
Medical Device Recall · March 26, 2026
Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
- Class II
Medical Device Recall · March 26, 2026
Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosisNeutralization Buffer may contain contaminants
- Class II
Medical Device Recall · March 26, 2026
Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
- Class II
Food Recall · March 26, 2026
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezerSoy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- Class II
Medical Device Recall · March 26, 2026
Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
- Class II
Medical Device Recall · March 26, 2026
Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
- Class II
Drug Recall · March 26, 2026
Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: Hetero, Hetero Labs Limited, Unit V, PolDiscoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
- Class II
Medical Device Recall · March 26, 2026
Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
- Class II
Medical Device Recall · March 26, 2026
Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
- Class II
Food Recall · March 26, 2026
Zarlengo's Double Dark Chocolate Gelato packaged in 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.
- Class II
Food Recall · March 26, 2026
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 terephtSoy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- Class II
Food Recall · March 26, 2026
Top Lid Label: Einstein Bros Bagels Honey Almond Double-Whipped Shmear. Cup Label: Plain Whipped Cream Cheese Spread. Net Wt 6 oz (170g). UPC 8 75343 00001 3. Keep Refrigerated. Made For EinsteUndeclared allergen (almond).
- Unclassified
Consumer Product Recall · March 26, 2026
Zhangzhou Qiangxing Supply Chain Management Co., Ltd. dba AirClub of China
AirClub Convertible BassinetsThe recalled convertible bassinets violate the mandatory standard for bedside sleepers because the mechanism used to attach the product to the adult bed creates an opening between the bedside sleeper and mattress, posing a deadly fall hazard to infants.
- Unclassified
Consumer Product Recall · March 26, 2026
Middle Way Electronics, of China
CCCEI Power StripsThe power strips do not contain supplementary overcurrent protection, which creates a risk of fire if the power strips are overloaded. The resulting fire can cause serious injury or death from smoke inhalation and burns.
- Unclassified
Consumer Product Recall · March 26, 2026
DuraTrac, of Anaheim, California
DuraTrac stainless steel gas connectorsThe recalled DuraTrac gas connectors contain a manufacturing defect that could cause a gas leak, posing a fire hazard to consumers.
- Unclassified
Consumer Product Recall · March 26, 2026
Shenzhen Luobei Trading Co., Ltd., of China
FUNTOK 24V 2-Seater Ride-On TrucksThe truck's circuit board can overheat and ignite, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · March 26, 2026
Guangzhou Aoran Trading Co., Ltd., dba Bioenrrty, of China
MPINOI Adult Portable Bed RailsThe 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 hazard warning labels.
- Unclassified
Consumer Product Recall · March 26, 2026
Petzl America, Inc., of Salt Lake City, Utah
Nomic and Ergonomic Ice Climbing AxesThe ice axe shaft can break at the handle during use, posing a fall hazard, which can result in serious injury or death.
- Unclassified
Consumer Product Recall · March 26, 2026
Huizhoushi Chuanglianxin Technology Co., Ltd, dba Sunnyyes, of China
Sunnyyes LED Mini LightsThe recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because the lights contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the screw used on the remote controls to secure the battery compartments that contain a lithium coin battery does not remain attached. Also, the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.Potential for product to contain foreign matter, confirmed to be inspect fragments.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-ZResorbable bone void filler falls outside standard specifications.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Drug Recall · March 25, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Fluocinonide, USP, 0.05% Cream, 60g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-138Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining eye and/or surrounding tissues during surgical procedures. These devices fall under the GMDN code 62478 entitled Ophthalmic soft-tissue surgical forceps, probe-like, single use . Double pouched in tyvek pouches, sold in boxes of 5 with an inner and outer box.
- Class II
Drug Recall · March 25, 2026
SUN PHARMACEUTICAL INDUSTRIES INC
Fluocinonide, USP, 0.05% Cream, 15g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-138Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
Olympus Corporation of the Americas
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-ELITE.Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class III
Medical Device Recall · March 25, 2026
Heraeus Medical GmbH (Dental Division)
Heraeus, PALAMIX uno. Material Number: 66057893.Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing process. Notification is to reduce the shelf life from 3 years to 1.5 years (17 months).
- Class II
Medical Device Recall · March 25, 2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-SField Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Class II
Medical Device Recall · March 25, 2026
BioCera Fibers, Bioresorbable Bone Void Filler, REF: ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KCResorbable bone void filler falls outside standard specifications.
- Class I
Medical Device Recall · March 25, 2026
Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number 258900029, LABEL, STERILE, IVSTATION SYRINGEPotential for mislabeled syringe produced by the i.v.STATION device.
- Class II
Food Recall · March 25, 2026
Bombay Kitchen brand Punjabi Mix; Net Wt 9oz (255g); INGREDIENTS: Chickpea Flour, Water, Non-GMO Expeller Pressed Canola Oil, Chana Dal (Split Bengal Gram), Brown Lentils (Masoor), Chickpeas, Rice FlaProduct(s) contain undeclared colors, FD&C Yellow #6 and FD&C Red #40