FoodFeb 13, 2019
Hy-Vee Stores HyVee brand Smores-flavored Bettercreme cheese cakes packaged recall — FDA F-0827-2019
Product contained an ingredient that tested positive for Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
Latest records
Latest recalls — page 1292
The newest recall records with useful source details are listed here.
FoodFeb 13, 2019
Spokane Produce -Washed and Packed Whole Green Lettuce Fillets, item # 80415 recall — FDA F-0847-2019
The green leaf lettuce fillets and heads are recalled due to a potential to be contaminated with E. Coli O157:H7.
Class IFDA: TerminatedSpokane Produce Inc.
FoodFeb 13, 2019
Hy-Vee Stores HyVee brand Pumpkin-fluff -flavored cheese cakes packaged in recall — FDA F-0826-2019
Product contained an ingredient that tested positive for Salmonella.
Class IFDA: TerminatedHy-Vee Stores Inc.
FoodFeb 13, 2019
Soom Foods 12 oz recall — FDA F-0783-2019
Soom Foods is recalling its tahini and chocolate tahini halva spread because their manufacturer, Achdut LTD. is recalling its Tahini products of all packages and sizes produced in the…
Class IFDA: TerminatedSoom Foods
DrugFeb 13, 2019
Lupin Pharmaceuticals Bimatoprost Ophthalmic Solution 0.03% recall — FDA D-0429-2019
Failed Impurities/Degradation Specifications: OOS results observed in any other individual impurity and total impurities.
Class IIIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugFeb 13, 2019
Hydrocortisone Cream 1% MS Anti itch Cream with Intensive Healing 2 oz tubes recall — FDA D-0426-2019
GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugFeb 13, 2019
US Pharmaceuticals Medline Remedy Essential Barrier Skin Protectant Ointment recall — FDA D-0427-2019
GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugFeb 13, 2019
US Pharmaceuticals Soothe & Cool Protect Moisture Guard Skin Protectant (petrolatum 59%),3.5 recall — FDA D-0425-2019
GMP Deviations: Out of specification results for Total Aerobic Microbial count in excipient purified water sample
Class IIFDA: TerminatedUS Pharmaceuticals Inc.
DrugFeb 13, 2019
Natures Rx the silver bullet 10x Capsules, 725 mg each recall — FDA D-0500-2019
Marketed without an Approved NDA/ANDA; FDA analysis found product to be tainted with undeclared sildenafil and tadalafil
Class IFDA: TerminatedNatures Rx
DrugFeb 13, 2019
Dymista recall — FDA D-0424-2019
Defective Container: Potential for broken glass in the neck area of the glass bottles.
Class IIFDA: TerminatedMylan Pharmaceuticals Inc.
VehicleFeb 13, 2019
BMW seats recall — NHTSA campaign 19V096000
BMW of North America, LLC (BMW) is recalling certain 2019 X5 xDrive40i and xDrive50i vehicles. The attachment bolts for the driver's seat and/or seat belt may not have been properly…
seatsBMW of North America, LLC
VehicleFeb 11, 2019
Ford instrument cluster/panel recall — NHTSA campaign 19V076000
Ford Motor Company (Ford) is recalling certain 2019 Ford Mustang, Lincoln Nautilus, and Lincoln Navigator vehicles. At vehicle start-up, the Instrument Panel Cluster Assembly (IPC) may not…
instrument cluster/panelFord Motor Company
Medical DeviceFeb 6, 2019
Medtronic Perfusion Systems RESERVOIR "Y" ADAPTER, (a) BT920 (b) BT926 Suction and recall — FDA Z-0785-2019
Medtronic discovered that certain Y-connectors included in the suction lines have exhibited tearing and cracking. These defects could cause the Y-connectors to leak when in use, which could…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceFeb 6, 2019
WEST PHARMA. SERVICES IL Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only recall — FDA Z-0768-2019
Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag is recalled due to similarities with 13mm Vial2Bag DC.
Class IFDA: TerminatedWEST PHARMA. SERVICES IL, LTD
Medical DeviceFeb 6, 2019
Haemonetics Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for recall — FDA Z-0778-2019
Haemonetics has received isolated reports that in some cases the 70ml centrifuge bowl may leak during cell salvage processing.
Class IIFDA: TerminatedHaemonetics Corporation
Medical DeviceFeb 6, 2019
XTANT MEDICAL Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC, REF recall — FDA Z-0790-2019
This recall has been initiated due to a change in packaging and sterilization method to address potential risks of compromised sterilization presented by the existing configuration.
Class IIFDA: TerminatedXTANT MEDICAL Inc.
Medical DeviceFeb 6, 2019
Roche Diagnostics Anti-HAV IgM test System, Material No. 11820591160 Product Usage: The recall — FDA Z-0784-2019
Potential for erroneous result messages for the Anti-HAV IgM assay when run on the cobas e 602 module. Discrepant result reporting may result.
Class IIFDA: TerminatedRoche Diagnostics Corporation
Medical DeviceFeb 6, 2019
Siemens Healthcare Diagnostics Atellica Sample Handler Prime recall — FDA Z-0783-2019
Multiple Issues Identified in Atellica Solution System Software in V 1.14.2 and lower in: Atellica IM 1300 Analyzer Atellica IM 1600 Analyzer;Atellica CH 930 Analyzer; Atellica Sample…
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceFeb 6, 2019
WEST PHARMA. SERVICES IL Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use recall — FDA Z-0769-2019
Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag DC 20mm is recalled due to similarities with 13mm Vial2Bag DC.
Class IFDA: TerminatedWEST PHARMA. SERVICES IL, LTD
Medical DeviceFeb 6, 2019
WEST PHARMA. SERVICES IL Vial2BAG DC 13mm, REF 6070111, Single use only, Rx Only recall — FDA Z-0767-2019
Adverse events have been reported with the use of oxytocin in conjunction with the product in pregnant women. There is a possibility that the device may cause inadequate admixing of drug…
Class IFDA: TerminatedWEST PHARMA. SERVICES IL, LTD
Medical DeviceFeb 6, 2019
3M Company - Health Care Business 3M(TM) Surgical Clipper by Remington(R) REF 9602 The 3M recall — FDA Z-0791-2019
3M has recently received reports involving the 3MTM Surgical Clipper by Remington, Model 9602, overheating in mobile/field EMS situations while charging from a modified sine wave power…
Class IIFDA: Terminated3M Company - Health Care Business
Medical DeviceFeb 6, 2019
Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 131VF7P Product Usage: The recall — FDA Z-0764-2019
These Swan Ganz catheters have incorrect lumen assembly, which causes reversal of the lumens. If the lumens are reversed the clinician may note reverse PA and CVP pressure values and…
Class IFDA: TerminatedEdwards Lifesciences, LLC
Medical DeviceFeb 6, 2019
Siemens Healthcare Diagnostics Atellica IM 1600 Analyzer: In vitro diagnostic testing of recall — FDA Z-0781-2019
Multiple Issues Identified in Atellica Solution System Software in V 1.14.2 and lower in: Atellica IM 1300 Analyzer Atellica IM 1600 Analyzer;Atellica CH 930 Analyzer; Atellica Sample…
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceFeb 6, 2019
Riverpoint Medical RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18 Product recall — FDA Z-0777-2019
Product is labeled with "CE", but is not yet approved in the European Union.
Class IIIFDA: TerminatedRiverpoint Medical, LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026184 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories