FoodApr 1, 2020
Winco Foods Blackberries, Raspberries and Blueberries), item# 107412 recall — FDA F-0857-2020
The product was found to be adulterated with Norovirus.
Class IIFDA: TerminatedWinco Foods LLC
Latest records
Latest recalls — page 1054
The newest recall records with useful source details are listed here.
FoodApr 1, 2020
Organic By Nature Pure Planet Organic Parasite Cleanse recall — FDA F-0904-2020
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
Class IIIFDA: TerminatedOrganic By Nature, Inc.
DrugApr 1, 2020
INFANTS ADVIL Ibuprofen 50 mg per 1.25 mL Oral Suspension Advil Infant Concentrated Drops recall — FDA D-1067-2020
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Class IIFDA: TerminatedGlaxosmithkline Consumer Healthcare Holdings
DrugApr 1, 2020
Glaxosmithkline Consumer Healthcare Holdings Advil Liqui-Gel Mini 160+20+20 CT (e-commerce) recall — FDA D-1069-2020
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Class IIFDA: TerminatedGlaxosmithkline Consumer Healthcare Holdings
DrugApr 1, 2020
Glaxosmithkline Consumer Healthcare Holdings Advil Sinus Congestion and Pain/Advil Allergy recall — FDA D-1068-2020
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Class IIFDA: TerminatedGlaxosmithkline Consumer Healthcare Holdings
DrugApr 1, 2020
ADVIL ALLERGY AND CONGESTION RELIEF Ibuprofen 200 mg Chlorpheniramine Maleate 4mg recall — FDA D-1065-2020
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Class IIFDA: TerminatedGlaxosmithkline Consumer Healthcare Holdings
DrugApr 1, 2020
ADVIL Ibuprofen 200 mg liquid filled capsules Advil Liqui-Gel Minis, 160 count bottle NDC recall — FDA D-1066-2020
Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.
Class IIFDA: TerminatedGlaxosmithkline Consumer Healthcare Holdings
DrugApr 1, 2020
Nostrum Laboratories Theophylline (Anhydrous) Extended-Release Tablets, 400 mg, 100-count recall — FDA D-1059-2020
CGMP Deviations: poor manufacturing practices resulted in Labeling: Incorrect or Missing Lot and/or Exp Date, product incorrectly labeled with incorrect lot and expiration date.
Class IIFDA: TerminatedNostrum Laboratories Inc.
VehicleMar 31, 2020
Crosstrek rear/other recall — NHTSA campaign 20V189000
Subaru of America, Inc. (Subaru) is recalling certain 2019 Crosstrek vehicles with rear seat belt assemblies with a dual-mode locking mechanism. The seat belt webbing sensor locking…
rear/otherSubaru of America, Inc.
VehicleMar 26, 2020
Chrysler differential unit recall — NHTSA campaign 20V183000
Chrysler (FCA US LLC) is recalling certain 2019 Jeep Grand Cherokee and Dodge Durango vehicles. The front differential may have been assembled with pinion gears that are insufficiently…
differential unitChrysler (FCA US LLC)
Medical DeviceMar 25, 2020
Siemens Medical Solutions USA Artis zee Biplane, Model No. 10094141 recall — FDA Z-1497-2020
A software issue could potentially cause the stand and table movements to be blocked.
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceMar 25, 2020
Stryker recall — FDA Z-1508-2020
Potential diff. in the length of the sheath tube and the sheath/probe. A diff. in length could lead to the base of the sheath/probe not being fully seated in the sheath tube which could…
Class IIFDA: TerminatedStryker Corporation
Medical DeviceMar 25, 2020
Smith & Nephew LEGION PS High Flex XLPE size 5-6 9mm Articular Insert recall — FDA Z-1507-2020
LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part
Class IIFDA: TerminatedSmith & Nephew, Inc.
Medical DeviceMar 25, 2020
Philips Allura Exper FD Series recall — FDA Z-1486-2020
A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
Class IIFDA: TerminatedPhilips North America, LLC
Medical DeviceMar 25, 2020
Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1516-2020
The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…
Class IIFDA: TerminatedAvid Medical, Inc.
Medical DeviceMar 25, 2020
Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1519-2020
The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…
Class IIFDA: TerminatedAvid Medical, Inc.
Medical DeviceMar 25, 2020
TeDan Surgical Innovations DS-0024 QUICK START DISTRACTION SCREW 14MM 5/BOX STERILE recall — FDA Z-1506-2020
The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product…
Class IIFDA: TerminatedTeDan Surgical Innovations LLC
Medical DeviceMar 25, 2020
Philips Allura CV20, system code 722031 recall — FDA Z-1493-2020
A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
Class IIFDA: TerminatedPhilips North America, LLC
Medical DeviceMar 25, 2020
Avid Medical Custom procedure trays containing medical components needed to facilitate recall — FDA Z-1520-2020
The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no…
Class IIFDA: TerminatedAvid Medical, Inc.
Medical DeviceMar 25, 2020
Boston Scientific, Implantable Cardioverter Defibrillator, DYNAGEN EL ICD DR, Model D152 recall — FDA Z-1512-2020
Boston Scientific released a new Software Update Application that was downloaded to four (4) distributed Model 3300 programmers. The Software Update Application then directed these…
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceMar 25, 2020
CRHF Medtronic CareLink Encore 29901 Programmer recall — FDA Z-1525-2020
Medtronic Conexus Telemetry has been determined to contain two primary cyber vulnerabilities: improper access control and the cleartext transmission of sensitive information.
Class IIFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceMar 25, 2020
Aesculap Implant Systems COLUMBUS REV F TIBIA OFFSET CEMENTED, Knee implant components recall — FDA Z-1482-2020
Low Density Polyethylene (LDPE) particles may be present on the surface of the implant upon the opening of the inner packaging.
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceMar 25, 2020
TeDan Surgical Innovations D-0012 3COR 12MM DISTRACTION SCREWS, 5/BOX, STERILE - Product recall — FDA Z-1503-2020
The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product…
Class IIFDA: TerminatedTeDan Surgical Innovations LLC
Medical DeviceMar 25, 2020
Aesculap Implant Systems AS COLUMBUS CR/PS TIB.PLAT.CEMENTED,Knee implant components recall — FDA Z-1481-2020
Low Density Polyethylene (LDPE) particles may be present on the surface of the implant upon the opening of the inner packaging.
Class IIFDA: TerminatedAesculap Implant Systems LLC
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Recent recall archives
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