FoodOct 21, 2020
Country Fresh Red Grapes 10oz UPC 68113118047 recall — FDA F-0081-2021
Potential to be contaminated with Listeria monocytogenes
Class IFDA: TerminatedCountry Fresh Inc.
Latest records
Latest recalls — page 955
The newest recall records with useful source details are listed here.
FoodOct 21, 2020
Country Fresh Apple Grape Tray With Caramel Sauce 2 lbs 10oz UPC 68113118012 recall — FDA F-0090-2021
Potential to be contaminated with Listeria monocytogenes
Class IFDA: TerminatedCountry Fresh Inc.
FoodOct 21, 2020
Lucky Spoon Bakery Gluten Free Chocolate Cupcakes with Vanilla recall — FDA F-0021-2021
Products are labeled gluten-free. A batch of flour from the raw material supplier tested positive for gluten so the firm immediately initiated a recall of the affected products.
Class IIFDA: TerminatedLucky Spoon Bakery, LLC
DrugOct 21, 2020
ASHTEL STUDIOS Smart Care HAND SANITIZER, Ethyl Alcohol 62% recall — FDA D-0098-2021
Labeling: Not Elsewhere Classified. Container packaging is made, formed or filled to be misleading, resembling food and drink pouches
Class IFDA: TerminatedASHTEL STUDIOS, Inc.
DrugOct 21, 2020
Cystaran recall — FDA D-0034-2021
Subpotent Drug: Product testing identified a decreased level of the active ingredient, Cysteamine HCl.
Class IIIFDA: TerminatedLeadiant Biosciences, Inc.
VehicleOct 19, 2020
Volkswagen Group of seats recall — NHTSA campaign 20V644000
Volkswagen Group of America, Inc. (Audi) is recalling one 2020 Audi Q3 vehicle. The driver's seat frame may have incorrectly been bolted to the seat rail.
seatsVolkswagen Group of America, Inc.
VehicleOct 15, 2020
Escape body control module/bcm recall — NHTSA campaign 20V635000
Ford Motor Company (Ford) is recalling certain 2020 Escape vehicles equipped with a key-start ignition system. The Body Control Module (BCM) intermittently may not pick up the signal from…
body control module/bcmFord Motor Company
VehicleOct 15, 2020
General Motors fuel pump recall — NHTSA campaign 20V639000
General Motors LLC (GM) is recalling certain 2020 Buick Enclave, Cadillac XT5, Cadillac XT6, Chevrolet Traverse, and GMC Acadia vehicles. The fuel pump's jet nozzle may have a plastic burr…
fuel pumpGeneral Motors LLC
VehicleOct 15, 2020
Paratransit column shift recall — NHTSA campaign 20V582000
Prime-Time Specialty Vehicles (Prime-Time) is recalling certain 2014-2019 Paratransit vehicles equipped with 3.6L engines. The transmission shifter cable may separate and disconnect from…
column shiftPrime-Time Specialty Vehicles
Medical DeviceOct 14, 2020
Biomet 3i CERTAIN BELLATEK TIN ABUTMENT 5.0MM Reference Number: IEDAN5 recall — FDA Z-0076-2021
Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the…
Class IIFDA: TerminatedBiomet 3i, LLC
Medical DeviceOct 14, 2020
Siemens Healthcare Diagnostics Dimension LOCI High Sensitivity Troponin I (TNIH) Flex recall — FDA Z-0052-2021
Positive bias across the Analytical Measurement Range of the TNIH assay compared to an unaffected control lot. The average bias observed for patient samples using lots EB0255 and EA0178 of…
Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.
Medical DeviceOct 14, 2020
Zimmer Biomet Dual Mobility Vivacit-E Bearing, Model Number 110031009 recall — FDA Z-0057-2021
The outer package is labeled as a Size C 38 mm, however, the implant inside the package is a Size E 42 mm.
Class IIFDA: TerminatedZimmer Biomet, Inc.
Medical DeviceOct 14, 2020
Medline Industries Kit Model #65193091, MTO Left Heart Kit - Product Usage: NAMIC Cath Lab recall — FDA Z-0068-2021
Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceOct 14, 2020
Ultradent Products PermaFlo Flowable Composite REF-UP 948 Shade: A2 - Product Usage: is a recall — FDA Z-0053-2021
Due to a potential manufacturing issue (cross contamination), composite is non-homogeneous.
Class IIFDA: TerminatedUltradent Products, Inc.
Medical DeviceOct 14, 2020
Medline Industries Kit Model #650305414, MTO Left Heart with DT Boulder Com Hosp - Product recall — FDA Z-0065-2021
Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceOct 14, 2020
Biomet 3i CERTAIN BELLATEK TITANIUM ABUTMENT 6.0MM Reference Number: IEDAT6 recall — FDA Z-0079-2021
Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the…
Class IIFDA: TerminatedBiomet 3i, LLC
Medical DeviceOct 14, 2020
Roche Diagnostics Operations BenchMark ULTRA Advanced Staining System (IVD)- Material recall — FDA Z-0085-2021
Potential for Fluid leaks within the instruments, creating an electrical short inside the power socket, which generates heat, smoke, and eventually burning and melting of the electrical…
Class IIFDA: OngoingRoche Diagnostics Operations, Inc.
Medical DeviceOct 14, 2020
Medline Industries ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR recall — FDA Z-0058-2021
There have been reports of the suction catheter coming apart from the device assembly during use.
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceOct 14, 2020
AB ULAX 1500 Flex Heat and Moisture Exchanger, Catalog Reference 150 - Product Usage: Heat recall — FDA Z-0059-2021
Firm has received 6 complaints that the Heat Moisture Exchanger (HME) disconnected from the closed respiratory circuit during use. If the HME separates, the ventilator circuit may not…
Class IIFDA: TerminatedAB ULAX
Medical DeviceOct 14, 2020
Biomet 3i BellaTek Encode Defin3DPMSERitive Abutments-3D Printed Model Reference Numbers recall — FDA Z-0073-2021
Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the…
Class IIFDA: TerminatedBiomet 3i, LLC
Medical DeviceOct 14, 2020
Roche Diagnostics Operations DISCOVERY ULTRA Advanced Staining System recall — FDA Z-0086-2021
Potential for Fluid leaks within the instruments, creating an electrical short inside the power socket, which generates heat, smoke, and eventually burning and melting of the electrical…
Class IIFDA: OngoingRoche Diagnostics Operations, Inc.
Medical DeviceOct 14, 2020
Medline Industries Kit Model #650301023, MTO Radiology Kit Cleveland Clinic - Product Usage recall — FDA Z-0063-2021
Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceOct 14, 2020
Medline Industries Kit Model #650304917, MTO Protection Station Plus with Drape - Product recall — FDA Z-0064-2021
Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceOct 14, 2020
Biomet 3i CERTAIN BELLATEK TITANIUM ABUTMENT 4.1MM Reference Number: IEDAT4 recall — FDA Z-0077-2021
Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees during manufacturing as compared with the provided patient scan data (Images may cause misalignment, the…
Class IIFDA: TerminatedBiomet 3i, LLC
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