Safety Recall Directory
Browse and filter the latest official safety alerts globally.
FDA DevicesCS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
FDA FoodFrederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.
Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.
Undeclared allergens (wheat and soy).
FDA FoodProspector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syrup, butter, vanilla, baking soda, sea salt, white chocolate (sugar, palm kernel fat, skimmed milk powder [12%], emulsifier [lecithins], natural vanilla flavoring), dark chocolate (sugar, palm kernel fat, fat reduced cocoa powder [20%], emulsifiers [lecithins], natural vanilla flavoring), pretzels (flour, water, salt, malt, dextrose, canola oil, yeast, soda), tofee bits (sugar, butter, almonds), coarse sea salt.; CONTAINS: MILK, TREE NUTS (ALMONDS), WHEAT; Produced in a facility that is shared with gluten, nuts, dairy, and soy.; Manufactured by: Prospector Popcord, LLC, Ridgefield, CT 06877; UPC: 850073852125
Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syrup, butter, vanilla, baking soda, sea salt, white chocolate (sugar, palm kernel fat, skimmed milk powder [12%], emulsifier [lecithins], natural vanilla flavoring), dark chocolate (sugar, palm kernel fat, fat reduced cocoa powder [20%], emulsifiers [lecithins], natural vanilla flavoring), pretzels (flour, water, salt, malt, dextrose, canola oil, yeast, soda), tofee bits (sugar, butter, almonds), coarse sea salt.; CONTAINS: MILK, TREE NUTS (ALMONDS), WHEAT; Produced in a facility that is shared with gluten, nuts, dairy, and soy.; Manufactured by: Prospector Popcord, LLC, Ridgefield, CT 06877; UPC: 850073852125
Products contain undeclared soy, specifically soy lecithin.
FDA FoodUncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamper resistant plastic container. UPC 812235023309. Distributed by: WE R NUTS LLC, 99 Seaview Blvd, Port Washington, NY 11050
Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamper resistant plastic container. UPC 812235023309. Distributed by: WE R NUTS LLC, 99 Seaview Blvd, Port Washington, NY 11050
Contains undeclared allergens (cashews, milk, and soy).
FDA DevicesMedline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B
Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B
Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA DevicesBrand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Description: 11-0494 - ICEMAN CLASSIC CUBE The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan¿ helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: no
Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Description: 11-0494 - ICEMAN CLASSIC CUBE The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan¿ helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: no
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
FDA DevicesDiowave Laser System, REF: Diowave 250W
Diowave Laser System, REF: Diowave 250W
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.
FDA DevicesRevolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23
Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23
GE 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.
FDA DevicesMedline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO KIT, Medline Kit Number/SKUVASC1057.
Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO KIT, Medline Kit Number/SKUVASC1057.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA DevicesArrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I
Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I
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.
FDA FoodDakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original - Salted Caramel - Cinnamon - Jalapeno. UPC 8 60010-57968 8. 4 - 4 oz (340g) jars. Net Wt 16 oz (454g). Produced in Winner, SD.
Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original - Salted Caramel - Cinnamon - Jalapeno. UPC 8 60010-57968 8. 4 - 4 oz (340g) jars. Net Wt 16 oz (454g). Produced in Winner, SD.
Foreign object (stainless steel dust/flakes or shreds of plastic)
FDA DevicesBARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
FDA FoodSwad Mango Flavored Masala Candy
Swad Mango Flavored Masala Candy
Contains undeclared Blue 1
FDA FoodKroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
FDA Food...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
Undeclared allergen ingredient (fish)
Germany BVLMönchshof Natur Radler Blutorange, 0,5 Liter
Mönchshof Natur Radler Blutorange, 0,5 Liter
Sonstige Gründe
FDA DevicesOn-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33
On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
FDA DevicesRevolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
GE 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.
FDA DevicesRevolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300
Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300
GE 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.
FDA DevicesRevolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27
Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27
GE 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.
Health CanadaExoplan
Exoplan
Performance
Health CanadaSprings Cellular Shades recalled due to choking hazard
Springs Cellular Shades recalled due to choking hazard
Choking hazard
Health CanadaTransport Canada Recall - 2026182 - DAIMLER TRUCK NORTH AMERICA
Transport Canada Recall - 2026182 - DAIMLER TRUCK NORTH AMERICA
Lights And Instruments
Health CanadaMicro Verdure brand Microgreens recalled due to pathogenic E. coli
Micro Verdure brand Microgreens recalled due to pathogenic E. coli
E. Coli - other pathogenic