FoodMar 1, 2017
Hy-Vee Stores Cr¿me De Menthe Almond Bark packaged 12 oz recall — FDA F-1489-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
Latest records
Latest recalls — page 1694
The newest recall records with useful source details are listed here.
FoodMar 1, 2017
Falafel King Tzatziki Sauce recall — FDA F-1527-2017
Falafel King announced a recall for their Tzatziki Sauce due to undeclared milk on product label.
Class IIFDA: TerminatedFalafel King Ent, Inc.
FoodMar 1, 2017
Hy-Vee Stores Candy packaged in a 9"/16oz recall — FDA F-1493-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co packaged cardboard boxes, UPC 77232-10880 recall — FDA F-1509-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co Trail's End Gourmet Chocolatey Crunch A) NET WT 18 recall — FDA F-1505-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Hy-Vee Stores Cookie & Candy packaged in a 9"/16oz recall — FDA F-1494-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co Palmer's Candies Game Day Party Bowl NET WT 16 OZ recall — FDA F-1500-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Hy-Vee Stores Chocolate almond bark packaged in 4 oz recall — FDA F-1487-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
FoodMar 1, 2017
Hy-Vee Stores Chocolate almond pretzels packaged in 4 oz recall — FDA F-1488-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co Palmer's Candies Drizzled Peanuts Brittle A) NET WT recall — FDA F-1499-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co packaged cardboard boxes, UPC 77232-10799 recall — FDA F-1512-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co NET WT 9 OZ recall — FDA F-1495-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co NET WT 9 OZ recall — FDA F-1497-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co Palmer's Candies Bakery Delights Christmas Tree recall — FDA F-1503-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co A) NET WT 9 OZ recall — FDA F-1498-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co Palmer's Candies Peppermint Bark A) NET WT 9 OZ recall — FDA F-1502-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
FoodMar 1, 2017
Palmer and Company, dba Palmer Candy Co UPC Code 77232-13990 recall — FDA F-1504-2017
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Class IFDA: TerminatedPalmer and Company, dba Palmer Candy Co
DrugMar 1, 2017
Sage Products Q Care Continue Care Kit for the non-ventilated patient recall — FDA D-0489-2017
Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of the Q Care Continue Care kit is printed with an expiration date of November 13, 2017; rather than the correct date…
Class IIIFDA: TerminatedSage Products Inc.
DrugMar 1, 2017
CycloSPORINE Capsules, USP, 100 mg, 30 count bottle recall — FDA D-0475-2017
Failed Impurities/Degradations Specifications; out of specification results for Maximum Unknown Impurities and Total Impurities.
Class IIFDA: TerminatedApotex Inc.
DrugMar 1, 2017
Sandoz Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 1 patch per pouch recall — FDA D-0481-2017
Labeling: Incorrect Instructions:outer carton contains the incorrect instructions for Step 2 stating "Do cut the patch" rather than the correct instructions of "Do not cut the patch". The…
Class IIFDA: TerminatedSandoz Inc.
Medical DeviceFeb 22, 2017
Mako Surgical Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The recall — FDA Z-1193-2017
Failure of the Offset Cup Reamer Handle not engaging its mating components.
Class IIFDA: TerminatedMako Surgical Corporation
Medical DeviceFeb 22, 2017
Philips Medical Systems (Cleveland) BrightView XCT recall — FDA Z-1186-2017
The intended use listed in the English and localized language IFUs for BrightView XCT systems did not match the intended use documented in the 510K submission.
Class IIFDA: TerminatedPhilips Medical Systems (Cleveland) Inc.
Medical DeviceFeb 22, 2017
Siemens Healthcare Diagnostics CentraLink Data Management System Software Versions recall — FDA Z-1204-2017
There is a remote possibility CentraLink may download an order to the ADVIA Automation System without specifying the sample type. This can occur when an order is received from the LIS…
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceFeb 22, 2017
GE Healthcare Discovery MR450 The systems are whole body magnetic resonance scanners recall — FDA Z-1188-2017
Potential safety issue with the patient bore heating on the Discovery MR450 narrow bore 1.5T MRI. In the event of a RF component failure, typically happening after extended system use, a…
Class IIFDA: TerminatedGE Healthcare, LLC
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