95,114 total recalls in our database
B&G Foods North America
Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds.
Wegmans Food Markets, Inc. voluntarily recalled fresh individually sold, bagged and sliced fresh plums, nectarines and peaches, peach salsa and several in-store baked desserts that may contain fresh peaches, nectarines, and/or plums. The fruit may be contaminated with Listeria monocytogenes.
Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds.
Tastefully Simple is recalling various lots of Cookie & Cream Fudge(Fabulous Fudge Gift) because the product appears to have mold growing on the small chocolate cookie pieces on the top of the Cookies & Cream Fudge.
NBTY has recalled ABC Dophlius Powder due to the presense of Rhizopus oryzae fungi.
KOZY SHACK, LLC has recalled Kozy Shack Simply Well Chocolate Pudding due to undeclared milk and lack of complete product labeling.
B&G Foods North America
Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds.
Wegmans Food Markets
Wegmans Food Markets, Inc. voluntarily recalled fresh individually sold, bagged and sliced fresh plums, nectarines and peaches, peach salsa and several in-store baked desserts that may contain fresh peaches, nectarines, and/or plums. The fruit may be contaminated with Listeria monocytogenes.
Zydus Pharmaceuticals USA
Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Failed Dissolution Specifications: Product was out of specification (OOS) at the 12 month long term stability testing point.
Failed USP Dissolution Test Requirements: This sub-recall is in response to Prometheus Laboratories Inc. recall for Mercaptopurine USP 50mg because the lot does not meet the specification for dissolution.
Defective Container: Glass vials may crack due to low (thin) out of specification vial wall thickness which may lead to contamination and lack of assurance of sterility.
Labeling:Missing Label: Bottles may not have a product label, or have a label with missing or illegible lot number and/or expiry date.
Lack of Assurance of Sterility; leaks were observed from the bag seam and port seal
The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods
The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods
When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion Quantification (aCMQ) applications, the reported End-Systolic Volume (ESV) may be smaller, and the Left Ventricular Ejection Fraction (EF) may be higher, than the ESV and EF calculated by manual tracing without the use of QLAB. An incorrect EF calculation could lead to misdiagnosis and/or delayed or incorrect therapy.
When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion Quantification (aCMQ) applications, the reported End-Systolic Volume (ESV) may be smaller, and the Left Ventricular Ejection Fraction (EF) may be higher, than the ESV and EF calculated by manual tracing without the use of QLAB. An incorrect EF calculation could lead to misdiagnosis and/or delayed or incorrect therapy.
The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods
The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods