Medical DeviceNov 19, 2025
Sonesta 6210 recall — FDA Z-0460-2026
Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.
Class IIFDA: OngoingSonesta Medical AB
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 22
Records are ordered by the best available source date.
Medical DeviceNov 19, 2025
GE Healthcare Finland Oy Carescape B450, Model no. 5805686 - shipped with potentially recall — FDA Z-0453-2026
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation…
Class IIFDA: OngoingGE Healthcare Finland Oy
Medical DeviceNov 19, 2025
Medline Industries Anesthesia Circuit Kits and other various kits that contain Anesthesia recall — FDA Z-0443-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Medline Industries Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY recall — FDA Z-0448-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Philips Medical Systems DMC GmbH CombiDiagnost R90 recall — FDA Z-0462-2026
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical…
Class IIFDA: OngoingPhilips Medical Systems DMC GmbH
Medical DeviceNov 19, 2025
Siemens Healthcare Diagnostics IMMULITE 2000 Oak Mix Specific Allergen recall — FDA Z-0491-2026
The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceNov 19, 2025
Medline Industries Convenience kits; DYNJ901047R ORTHO SPINE FUMICH DYNJ902308K TOTAL JOINT recall — FDA Z-0451-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
GE Healthcare Finland Oy BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected recall — FDA Z-0457-2026
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation…
Class IIFDA: OngoingGE Healthcare Finland Oy
Medical DeviceNov 19, 2025
Medline RenewalLigasure Blunt Tip Sealer/Divider, NanoCoated Compatible with FT10 Generator recall — FDA Z-0472-2026
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Alinity hq Analyzer recall — FDA Z-0489-2026
Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results.
Class IIFDA: OngoingAbbott Laboratories
Medical DeviceNov 19, 2025
Philips Medical Systems DMC GmbH ProxiDiagnost N90 recall — FDA Z-0461-2026
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical…
Class IIFDA: OngoingPhilips Medical Systems DMC GmbH
Medical DeviceNov 19, 2025
Medline Industries Convenience Kit, BREAST HERNIA DYNJ909125G recall — FDA Z-0447-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Siemens Healthcare Diagnostics 3gAllergy Specific IgE Universal Kit recall — FDA Z-0492-2026
The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceNov 19, 2025
Medline Industries Anesthesia Circuit Kits and other various kits that contain Anesthesia recall — FDA Z-0445-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Olympus Single Use Single Use Electrosurgical Snare SD-400 Single Use Single Use recall — FDA Z-0483-2026
Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceNov 19, 2025
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin) recall — FDA Z-0485-2026
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
Class IIFDA: OngoingCovidien, LP
Medical DeviceNov 19, 2025
Medline Industries DYNJ909119G ROBOTIC GASTRIC LAP SLEEVE-LF DYNJ909127F CYSTO DYNJ909129D recall — FDA Z-0446-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Medline Industries Anesthesia Circuit Kits and other various kits that contain Anesthesia recall — FDA Z-0442-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
GE Healthcare Finland Oy Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient recall — FDA Z-0456-2026
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation…
Class IIFDA: OngoingGE Healthcare Finland Oy
Medical DeviceNov 19, 2025
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator recall — FDA Z-0473-2026
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Abbott Medical Liberta RC DBS IPG recall — FDA Z-0459-2026
There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse…
Class IIFDA: OngoingAbbott Medical
Medical DeviceNov 19, 2025
TECHNO-PATH MANUFACTURING Multichem ID-B recall — FDA Z-0502-2026
Potential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform.
Class IIFDA: OngoingTECHNO-PATH MANUFACTURING LTD.
Medical DeviceNov 19, 2025
Abbott Medical Eterna SCS IPG recall — FDA Z-0458-2026
There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse…
Class IIFDA: OngoingAbbott Medical
Medical DeviceNov 19, 2025
Accriva Diagnostics VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code recall — FDA Z-0500-2026
Due to an device without a premarket clearance being incorrectly package and distributed.
Class IIIFDA: OngoingAccriva Diagnostics, Inc.
About the 2025 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.