Medical DeviceOct 30, 2024
smiths medical portex, Nasopharyngeal Airway, Sizes as follows: a) AIRWAY NASOPHARYNGEAL recall — FDA Z-0143-2025
Uncertainty in the seal integrity of the sterile packaging.
Class IIFDA: OngoingSmiths Medical ASD Inc.
Latest records
Latest recalls — page 313
The newest recall records with useful source details are listed here.
Medical DeviceOct 30, 2024
Medline AMBULATORY MINI PACK, REF DYNJ82579 recall — FDA Z-0172-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Stopcock w/Ext. 10/EA, Product Code REF MXG300242 recall — FDA Z-0202-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Olympus Corporation of the Americas EZDilate Wire Guided Balloon- Indicated for use in adult recall — FDA Z-0225-2025
Mislabeled Glo Cath Label (attached to the device) states: 11 mm, 12 mm, 13 mm however the balloon is 8.5mm, 9.5mm and 10.5 mm and may result in prolonged surgery. All other labeling is…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceOct 30, 2024
Polymer Technology Systems, Inc. dba PTS A1CNow+ Multi-Test HbA1c System consists of (1) a recall — FDA Z-0223-2025
The reason for this recall is PTS Diagnostics, Inc. received complaints of non-matching cartridge and analyzer codes within the product test system box. Use of cartridges and analyzers with…
Class IIFDA: CompletedPolymer Technology Systems, Inc. dba PTS Diagnostics,…
Medical DeviceOct 30, 2024
Medline EYE PACK, REF LYN036EPESB recall — FDA Z-0180-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
MEDLINE INDUSTRIES, LP - Northfield Centurion OB TRAY, REF MNS13965A recall — FDA Z-0151-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Datex-Ohmeda Aespire 100. This anesthesia gas machine is intended to provide general recall — FDA Z-0075-2025
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Class IFDA: OngoingDatex-Ohmeda, Inc.
Medical DeviceOct 30, 2024
Medline brand, medical procedure convenience kits, labeled as: a) CUH OPEN HEART A B C recall — FDA Z-0156-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Medline DENTAL PACK, REF DYNJ64086B recall — FDA Z-0159-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar DPT w/Stopcock & 3cc Flush 10/EA, Product Code REF recall — FDA Z-0193-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
smiths medical SurgiVet Advisor Tech Accessories, Product Code REF V2714 recall — FDA Z-0205-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex Arterial Kit 1/EA, Product Code REF MX7827 recall — FDA Z-0187-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Medline CHEST TUBE INSERTION TRAY ADUL, REF CHT1165 recall — FDA Z-0167-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) TRAY ADD A CATH FOL UM MF recall — FDA Z-0164-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) PLASTIC PACK, REF recall — FDA Z-0165-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Datex-Ohmeda Aisys CS2 with Et Control recall — FDA Z-0083-2025
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Class IFDA: OngoingDatex-Ohmeda, Inc.
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) LITHOTOMY PACK, REF recall — FDA Z-0175-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
FoodOct 30, 2024
Youngstown Grape Distributors Farmers Juice Watermelon Hydration packaged in a 12 fl recall — FDA F-0062-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
FoodOct 30, 2024
Choi's Kimchi packaged 16oz plastic pouch with spout, keep refrigerated recall — FDA F-0055-2025
Salmonella.
Class IFDA: TerminatedChoi's Kimchi LLC
FoodOct 30, 2024
Youngstown Grape Distributors Farmers Juice Focus Greens packaged in a 12 fl recall — FDA F-0060-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
FoodOct 30, 2024
Youngstown Grape Distributors Happy Moose Juice Tropical Roots packaged in a plastic 12 fl recall — FDA F-0058-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
FoodOct 30, 2024
Salt City Baking Company Sour Charlie bread, #2092, bag of 6 rolls recall — FDA F-0057-2025
Undeclared Wheat flour. Product contains wheat flour but product was sold without the Ingredients Statement.
Class IIFDA: TerminatedSalt City Baking Company, LLC
FoodOct 30, 2024
Horizon Organic Dairy refrigerated, One Pint recall — FDA F-0064-2025
Potential for premature product spoilage during shelf life.
Class IIFDA: TerminatedHorizon Organic Dairy, LLC
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September 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 categoriesOctober 2025455 records · 4 categories