FoodFeb 25, 2026
Lotus Mom Corporation dba Indian Kitchen Mart IKM Aluminum Saucepan 9" with Wooden Handle recall — FDA H-0511-2026
Potential contamination with leachable lead.
Class IIFDA: OngoingLotus Mom Corporation dba Indian Kitchen Mart
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
September 2026300 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 categories
2026 recalls — page 99
Records are ordered by the best available source date.
FoodFeb 25, 2026
H & N Group Tail Off-White Shrimp recall — FDA H-0516-2026
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Class IIFDA: TerminatedH & N Group Inc.
FoodFeb 25, 2026
Reser's Fine Foods The Tuna Salad product container is mislabeled with a Chicken recall — FDA H-0517-2026
Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
Class IFDA: TerminatedReser's Fine Foods, Inc.
FoodFeb 25, 2026
Pure Solutions Net Wt., 1 fl oz recall — FDA H-0537-2026
Label declares bovine colostrum but does not declare milk allergen.
Class IIFDA: OngoingPure Solutions, Inc.
FoodFeb 25, 2026
Art Monkey LLC dba Why Not Natural Why Not Natural Moringa Capsules 120 capsule bottle recall — FDA H-0510-2026
Potential to be contaminated with Salmonella
Class IFDA: TerminatedArt Monkey LLC dba Why Not Natural
FoodFeb 25, 2026
Lotus Mom Corporation dba Indian Kitchen Mart Brass Pital Pot 4-quart recall — FDA H-0514-2026
Potential contamination with leachable lead.
Class IFDA: OngoingLotus Mom Corporation dba Indian Kitchen Mart
VehicleFeb 23, 2026
Telluride recliner recall — NHTSA campaign 26V105000
Kia America, Inc. (Kia) is recalling certain 2025 Telluride vehicles, equipped with power front seat(s). Due to a manufacturing error, the driver and passenger seat back frame assemblies…
reclinerKia America, Inc.
VehicleFeb 20, 2026
Explorer rear recall — NHTSA campaign 26V101000
Ford Motor Company (Ford) is recalling certain 2017-2019 Explorer vehicles. The rear suspension toe links may fracture.
rearFord Motor Company
VehicleFeb 20, 2026
Ford integrated trailer brake control recall — NHTSA campaign 26V104000
Ford Motor Company (Ford) is recalling certain 2021-2026 F-150, 2022-2026 F-250 SD, F-350 SD, F-450 SD, F-550 SD, Maverick, 2024-2026 Ranger, 2023-2026 F-600 SD, 2022-2027 Lincoln…
integrated trailer brake controlFord Motor Company
Medical DeviceFeb 18, 2026
Philips Spectral CT 7500 on Rails recall — FDA Z-1318-2026
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to…
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceFeb 18, 2026
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B recall — FDA Z-1336-2026
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x recall — FDA Z-1323-2026
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109 recall — FDA Z-1327-2026
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088 recall — FDA Z-1333-2026
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline Industries Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters recall — FDA Z-1321-2026
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline Industries 1) UNIVERSAL KIT, Kit SKU DT22010B recall — FDA Z-1330-2026
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710 recall — FDA Z-1329-2026
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline Industries Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound recall — FDA Z-1324-2026
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A recall — FDA Z-1335-2026
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Alphatec Spine ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF recall — FDA Z-1342-2026
Due a design issue where the navigated array connection geometry is incorrect.
Class IIFDA: OngoingAlphatec Spine, Inc.
Medical DeviceFeb 18, 2026
Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor recall — FDA Z-1360-2026
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
Class IIIFDA: OngoingSUREPULSE MEDICAL LTD
Medical DeviceFeb 18, 2026
Medline Industries Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B recall — FDA Z-1313-2026
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 18, 2026
Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor recall — FDA Z-1356-2026
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
Class IIIFDA: OngoingSUREPULSE MEDICAL LTD
Medical DeviceFeb 18, 2026
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion 5 M20 System Model Numbers: (1)722228 recall — FDA Z-1351-2026
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.