Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,601–11,650 of 15,364
- Class II
Food Recall · June 13, 2024
The Frozen Farmer Santa's Cookies Ice Cream Cookie Sandwich the Elf On the Shelf 4 fl oz UPC 850023398178. Individually wrapped in plastic, 4 sandwiches packaged in a cardboard box, 24 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
LaSalle Chocolate Ice Cream 16 fl oz/1 pint, UPC 671891374114. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Hershey s Ice Cream Cookies & Cream Polar bear Premium Ice Cream Sandwich 45 oz/4 fl oz UPC 24682312855. Individually wrapped in plastic and packaged in cardboard box, 24 units per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Yelloh! Chocolate Chip Ice Cream Sandwich With Vanilla Ice Cream 24 fl oz UPC 810038685106. Individually wrapped in plastic. 6 sandwiches packaged in cardboard box, 12 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Dolcezza Peanut Butter Cup Gelato 16 fl oz/1 pint, UPC 857838006472. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Abilyn s Frozen Bakery Ice Cream Cake Vanilla & Chocolate 6", UPC 851545008002. Packaged in cardboard box, 3 boxes per case. Abilyn s Frozen Bakery Ice Cream Cake Vanilla & Chocolate 8", UPC 851545008Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Jeni's Ice Cream Sandwiches Triple Berry Tart 3.5 fl oz UPC 858241006851. Individually wrapped in plastic and packaged in cardboard box, 3 sandwiches per box. 8 boxes per case.Possible contamination with Listeria monocytogenes
- Unclassified
Consumer Product Recall · June 13, 2024
Adven Group, dba Nap Queen Sleep, of Missouri City, Texas
Nap Queen Sleep Victoria Hybrid MattressesThe recalled mattresses violate mandatory federal flammability regulations for mattresses, posing a fire hazard to consumers.
- Unclassified
Consumer Product Recall · June 13, 2024
Black Diamond Equipment, of Salt Lake City, Utah
Neve Strap Crampons and Accessory KitsThe screws that connect the plastic heel cup to the aluminum heel unit of the crampon can loosen and allow the heel cup to detach from the crampon, posing a fall hazard.
- Class II
Food Recall · June 13, 2024
Cumberland Farms Farmhouse Premium Ice Cream Sandwich, Rich Vanilla, 4 fl oz UPC 42704010046. Individually wrapped in plastic, 24 units per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Dolcezza Hot Cocoa Gelato 16 fl oz/1 pint, UPC 857838006610. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Dolcezza Sugar Cookie Dough Gelato 16 fl oz/1 pint, UPC 857838006618. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Hershey s Ice Cream Vanilla & Chocolate Flavored Ice Cream Sheet Cake 110 fl oz, UPC 24682060152. Packaged in cardboard box, 3 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Amafruit Superfruits from the Amazon Organic Acai packaged in 3 gallon plastic tubs, UPC 855738002181.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Yelloh! Vanilla Fudge Sundae Cones 4 fl oz UPC 810038684901. 12 cones wrapped in paper, packaged in cardboard box, 8 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Marco Green Tea White Chocolate Ice Cream 16 fl oz/1 pint, UPC 860006880521. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Dolcezza Dark Chocolate Gelato 16 fl oz/1 pint, UPC 857838006083. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
The Frozen Farms Farm Crafted Watermelon Sorbet 16 fl oz/1 pint, UPC 850023398024. Packaged in paper containers, 8 containers per casePossible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Abilyn s Frozen Bakery Ice Cream Cake For the Love of Chocolate 6", UPC 851545008057. Packaged in cardboard box, 4 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Abilyn's Frozen Bakery Cookie Dough Ice Cream UPC 851545008071. Packaged in cardboard box, 4 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Hershey's Ice Cream Cookies and Cream Ice Cream Cone 4 fl oz UPC 24682313067. Individually packaged in paper. 3 sandwiches per box. 24 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Dolcezza Swiss Chocolate 16 fl oz/1 pint, UPC 857838006342. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Chipwich Double Chocolate Chip Ice Cream Sandwich 4 fl oz, UPC 810493030329. Individually plastic wrapped sandwiches packaged in a carboard box. 12 boxes per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Dolcezza Mascarpone & Berries Gelato 16 fl oz/1 pint, UPC 857838006083. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Chipwich Mint Chocolate Chip Ice Cream 16 fl oz/1 pint, UPC 810493032026. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · June 13, 2024
Taharka Honey Graham Ice Cream 16 fl oz/1 pint, UPC 638455788442. Packaged in paper containers, 8 containers per case.Possible contamination with Listeria monocytogenes
- Unclassified
Consumer Product Recall · June 13, 2024
Amana, Daikin, and Goodman branded air conditioning and heat pump packaged unitsThe unit's serial plate can have incorrect electrical ratings which can lead to incorrect wirings being used, posing a fire hazard.
- Unclassified
Consumer Product Recall · June 13, 2024
Outad Good Life Ltd., of China
1 Set Puzzle "Magnetic", "Magnetism", or "Magnetism Intelligence Strategy Game" Magnetic Battle Chess GamesThe recalled magnetic chess games, which include 20 magnet pieces, violate the mandatory federal toy magnet regulation because the set contains one or more magnets that fit within CPSC's small parts cylinder, and the magnets are stronger than permitted. When high-powered magnets are swallowed, the ingested magnets can attract each other, or another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.
- Unclassified
Consumer Product Recall · June 13, 2024
Southern Telecom Inc., of New York
Lomi Roll-On Waxing KitsThe roll-on warmer's power cord can overheat and short circuit, posing fire, burn, and electrical shock hazards.
- Class I
Food Recall · June 12, 2024
SAVPAK Duro 10x10, 8oz plastic bag, DISTRIBUTED BY: Southcoast Product Inc. Dallas, Texas 75215; UPC 29661 00076.Undeclared Wheat Allergen
- Class II
Food Recall · June 12, 2024
Fresh Catch Inc. Yellowfin Tuna, 1 loin per case packaged in carboard boxes with keep refrigerated labelHigh histamine levels in Yellowfin Tuna
- Class I
Medical Device Recall · June 12, 2024
BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)Sterilization certificates could not be validated by the supplier
- Class I
Medical Device Recall · June 12, 2024
BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)Sterilization certificates could not be validated by the supplier
- Class I
Medical Device Recall · June 12, 2024
BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)Sterilization certificates could not be validated by the supplier
- Class II
Drug Recall · June 12, 2024
Zilretta (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for: Pacira Pharmaceuticals Inc., San Diego, CA 92121, NDC 65250-003-01 (carton) NDC 65Failed Dissolution Specifications - did not meet the acceptance criteria for IVR Level 3 testing at 9 months 2-8¿C followed by 6 weeks at 25¿C
- Class I
Food Recall · June 12, 2024
SAVPAK Duro Rueda 8oz, plastic bag, DISTRIBUTED BY: Southcoast Produce Inc. Dallas, Texas 75215; UPC 29661 00073Undeclared Wheat Allergen
- Class II
Medical Device Recall · June 12, 2024
Autotome RX 20mm CUT WIRE Cannulating Sphincterotome, Material Number (UPN) M00545170. The device is used in selective cannulation of the bile duct.Foreign material may be present on the enclosed section of the cutting wire which may lead to inability to optimally bow the sphincterotome. This issue may lead to prolongation of procedure.
- Class I
Medical Device Recall · June 12, 2024
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)Sterilization certificates could not be validated by the supplier
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Outake, REF CET200 and CET300, The Catheter Extractor is a catheter accessory dMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG/Worley advanced CSG (Introducer Catheter kit), REF: FCL-083-02/A WMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Ethicon Sarl, a Johnson & Johnson Company
SURGICEL FIBRILLAR 1INX2IN(2.5CMX5.1CM), Product Number: 1961Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Custom Procedure Kit (Angiography/Angioplasty kit), REF: OPT0242-00 S1279-01 S29Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K02 (Custom Syringe Kit), REF: K02-00873A, Inject fluids into, or withdraw fluiMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: PC (Pericardiocentesis Tray - Fluid drainage tray), REF: PC101/B PC801 PC801/AMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K11 (Custom Pressure Monitoring Kit), REF: K11-00382C To support fluid administMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid Response Waste Management System Kit, REF BRC-BAL-INT-SL/B An endoscope anMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG (Introducer Catheter), REF: FCL-069-00/A FCL-069-02/A FCL-069-03/Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Medical Action Industries, Inc. 306
Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250 each/case), 6141 (250 each/case), 6203 (40 each/case), 6805 (50The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Customer Procedure Kit (Angiography/Angioplasty kit), REF: K05-02166B K05T-00380C K05TMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
- Class II
Medical Device Recall · June 11, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K10/K10-PI (Custom Waste Management Kit), REF: K10T-05815 K10T-05816 K10-04722CMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.