Medical DeviceFeb 25, 2026
Integra LifeSciences Private Label CVS recall — FDA Z-1365-2026
Potential packaging failures, which could lead to a breach in the sterile barrier.
Class IIFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categories
2026 recalls — page 78
Records are ordered by the best available source date.
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) BAP NORTH ROBOTIC SURGERY CDS recall — FDA Z-1419-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Auris Health MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R recall — FDA Z-1383-2026
Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading, application will…
Class IIFDA: OngoingAuris Health, Inc
Medical DeviceFeb 25, 2026
Wilson-Cook Medical Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 recall — FDA Z-1362-2026
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.
Class IIFDA: OngoingWilson-Cook Medical Inc.
Medical DeviceFeb 25, 2026
Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN recall — FDA Z-1366-2026
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) ADMIT KIT recall — FDA Z-1410-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) LVAD DRIVELINE TRAY recall — FDA Z-1402-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall — FDA Z-1406-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) KIT ACES INSERT PEG recall — FDA Z-1401-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Integra LifeSciences MediHoney Gel with Active Leptospermum Honey recall — FDA Z-1363-2026
Potential packaging failures, which could lead to a breach in the sterile barrier.
Class IIFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Medical DeviceFeb 25, 2026
Bard Peripheral Vascular Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff recall — FDA Z-1367-2026
Due to damage to outer tray that can potentially compromise the sterile barrier
Class IIFDA: OngoingBard Peripheral Vascular Inc
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall — FDA Z-1407-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 25, 2026
Immunotech A.S Estrone RIA, REF: DSL8700 recall — FDA Z-1369-2026
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.
Class IIFDA: OngoingImmunotech A.S.
Medical DeviceFeb 25, 2026
Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall — FDA Z-1392-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
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
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 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
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.