FoodMay 27, 2020
Condies Foods 43559 SNDW Chicken Sandwich on White Single, vacuumed pack recall — FDA F-0948-2020
Undeclared SOY allergen. Wrong ingredient purchased and used.
Class IFDA: TerminatedCondies Foods, Inc.
Latest records
Latest recalls — page 1027
The newest recall records with useful source details are listed here.
FoodMay 27, 2020
Frito-Lay Ruffles Ranch flavoured dip 425 g recall — FDA F-0957-2020
Potential to be contaminated with mold
Class IIFDA: TerminatedFrito-Lay, Inc.
FoodMay 27, 2020
Willamette Valley Pie Company, LLC packaged in clamshells container, six containers per case recall — FDA F-0970-2020
Cherry Pie packages were recalled due to being misbranded. The actual product inside clamshell package is Raspberry Rhubarb Pie, but it was mislabeled as Cherry Pie. Raspberry Rhubarb Pie…
Class IIFDA: TerminatedWillamette Valley Pie Company, LLC.
FoodMay 27, 2020
Willamette Valley Pie Company, LLC packaged in clamshells container, six containers per case recall — FDA F-0969-2020
Raspberry Rhubarb Pie packages were recalled due to undeclared artificial almond. The actual product inside a clamshell package is Cherry Pie, which contains artificial almond extract, but…
Class IIFDA: TerminatedWillamette Valley Pie Company, LLC.
DrugMay 27, 2020
Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial recall — FDA D-1271-2020
Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.
Class IIFDA: TerminatedMylan Institutional LLC
DrugMay 27, 2020
Gabapentin Tablets USP, 600 mg recall — FDA D-1272-2020
Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
Class IIIFDA: TerminatedInvaGen Pharmaceuticals, Inc.
VehicleMay 27, 2020
Mustang camera recall — NHTSA campaign 20V306000
Ford Motor Company (Ford) is recalling certain 2020 Mustang vehicles equipped a forward-looking camera. The camera may be misaligned to the vehicle and features that are dependent on the…
cameraFord Motor Company
VehicleMay 21, 2020
Chevrolet Trailblazer tires recall — NHTSA campaign 20V295000
General Motors LLC (GM) is recalling certain 2021 Chevrolet Trailblazer vehicles factory-equipped with optional 17-inch sport terrain tires. The certification label on these vehicles does…
tiresGeneral Motors LLC
Medical DeviceMay 20, 2020
Argon Medical Devices Arterial Line Kit 20ga X 3", Model 498411B, Rx Only, Sterile EO, UDI recall — FDA Z-1936-2020
Arterial Line Kits include thicker curved reverse-cutting needle with a 0-silk suture, instead of the usual straight-cutting needle with a 3-0 silk suture. The thicker suture may be more…
Class IIFDA: TerminatedArgon Medical Devices, Inc.
Medical DeviceMay 20, 2020
Access Scientific BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm recall — FDA Z-1977-2020
Saline Flush Syringe compromised sterility due to holes in the packaging.
Class IIFDA: TerminatedAccess Scientific LLC
Medical DeviceMay 20, 2020
Access Scientific BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 3Fr 6cm recall — FDA Z-1980-2020
Saline Flush Syringe compromised sterility due to holes in the packaging.
Class IIFDA: TerminatedAccess Scientific LLC
Medical DeviceMay 20, 2020
W. L. Gore & Associates Gore DrySeal Flex Introducer Sheath, Catalog #DSF1433, 33cm 14FR recall — FDA Z-1962-2020
The devices were mislabeled with the incorrect product size resulting in 16Fr devices being labeled as 14Fr devices.
Class IIFDA: TerminatedW. L. Gore & Associates Inc.
Medical DeviceMay 20, 2020
Cardiac Assist TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15, Product recall — FDA Z-1949-2020
Failure to prime due to an assembly error
Class IIFDA: TerminatedCardiac Assist, Inc.
Medical DeviceMay 20, 2020
Cardiac Assist TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD, Product recall — FDA Z-1953-2020
Failure to prime due to an assembly error
Class IIFDA: TerminatedCardiac Assist, Inc.
Medical DeviceMay 20, 2020
Beckman Coulter iQ200 Series Urine Microscopy Analyzer- All part numbers recall — FDA Z-1945-2020
A defect in the SATA power adapter cable within the instrument s computer has the potential risk for an electrical short that may lead to the following outcomes: charring and/or melting of…
Class IIFDA: TerminatedBeckman Coulter Inc.
Medical DeviceMay 20, 2020
ICU Medical Central Venous Catheters are indicated for the assessment of hemodynamic status recall — FDA Z-2000-2020
Inability for the guidewire to pass through the needles included with the catheter kits.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceMay 20, 2020
Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a recall — FDA Z-1935-2020
Ambulance Cots may not meet crash test standard BS EN 1789
Class IIFDA: TerminatedStryker Medical Division of Stryker Corporation
Medical DeviceMay 20, 2020
Siemens Cios Spin VA30-mobile X-Ray system, Material # 10308194 - Product Usage: The Cios recall — FDA Z-1959-2020
Main cable can be plugged or unplugged from the X10 connector which is part of the main unit (c-arm) at any time during clinical session. If the system displays the error message Err 16305…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceMay 20, 2020
ICU Medical Central Venous Catheters are indicated for the assessment of hemodynamic status recall — FDA Z-1999-2020
Inability for the guidewire to pass through the needles included with the catheter kits.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceMay 20, 2020
ICU Medical Central Venous Catheters are indicated for the assessment of hemodynamic status recall — FDA Z-1997-2020
Inability for the guidewire to pass through the needles included with the catheter kits.
Class IIFDA: TerminatedICU Medical, Inc.
Medical DeviceMay 20, 2020
Covidien Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray 400mL, 16 recall — FDA Z-1992-2020
Temperature sensing catheters failed to meet the established calibrated temperature sensing tolerance of +/- 0.2¿C. Failure to correctly measure patient body temperatures could lead to an…
Class IIFDA: TerminatedCovidien LLC
Medical DeviceMay 20, 2020
Cardiac Assist TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000 recall — FDA Z-1955-2020
Failure to prime due to an assembly error
Class IIFDA: TerminatedCardiac Assist, Inc.
Medical DeviceMay 20, 2020
The Magstim Company Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the recall — FDA Z-1966-2020
It was identified that there is a potential for the Stim Interconnecting high Voltage Cable located at the rear of the Rapid2 and Horizon power supply unit to fail.
Class IIFDA: TerminatedThe Magstim Company Limited
Medical DeviceMay 20, 2020
Handicare AB EVA Floor Lifts, Model Numbers: 400, 450, 600 recall — FDA Z-1943-2020
After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to…
Class IIFDA: OngoingHandicare AB
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026180 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