Medical DeviceFeb 4, 2026
Broselow Pediatric Emergency Rainbow Tape recall — FDA Z-1114-2026
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Class IFDA: OngoingSunMed Holdings, LLC
February 2026 recalls — page 12
These records include useful source details for the selected month.
Medical DeviceFeb 4, 2026
Philips Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version recall — FDA Z-1206-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU recall — FDA Z-1188-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Canon Medical System, USA Alphenix INFX-8000V, interventional fluoroscopic x-ray system recall — FDA Z-1179-2026
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceFeb 4, 2026
Siemens Medical Solutions USA Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall — FDA Z-1175-2026
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceFeb 4, 2026
Canon Medical System, USA Alphenix INFX-8000H, interventional fluoroscopic x-ray system recall — FDA Z-1178-2026
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceFeb 4, 2026
Broselow recall — FDA Z-1117-2026
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Class IFDA: OngoingSunMed Holdings, LLC
Medical DeviceFeb 4, 2026
GOLD STAR DISTRIBUTION Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN recall — FDA Z-1181-2026
Potential exposure of rodents and rodent activity in the distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION Inc.
Medical DeviceFeb 4, 2026
Broselow Domestic Complete ALS Organizer recall — FDA Z-1116-2026
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Class IFDA: OngoingSunMed Holdings, LLC
Medical DeviceFeb 4, 2026
Philips Upgrade to MR 7700 recall — FDA Z-1214-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF, Kit recall — FDA Z-1197-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Philips Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems recall — FDA Z-1211-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF, Kit SKU recall — FDA Z-1196-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF, Kit recall — FDA Z-1187-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Philips Ingenia Ambition X recall — FDA Z-1210-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Philips SmartPath to dStream for XR and 3.0T recall — FDA Z-1216-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Zimmer Tourniquet Systems A.T.S.¿ 5000TS Tourniquet Systems recall — FDA Z-1201-2026
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device…
Class IIFDA: OngoingZimmer Surgical Inc.
Medical DeviceFeb 4, 2026
Canon Medical System, USA Alphenix INFX-8000F, interventional fluoroscopic x-ray system recall — FDA Z-1177-2026
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK, Kit SKU DYNJ35494C recall — FDA Z-1199-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Philips Evolution Upgrade 3.0T recall — FDA Z-1205-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
GOLD STAR DISTRIBUTION Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT recall — FDA Z-1183-2026
Potential exposure of rodents and rodent activity in the distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION Inc.
Medical DeviceFeb 4, 2026
Philips Ingenia Elition X. Product Code (REF): (1) 781358, (2) 782107, (3) 782136. MR recall — FDA Z-1212-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
GOLD STAR DISTRIBUTION Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS recall — FDA Z-1182-2026
Potential exposure of rodents and rodent activity in the distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION Inc.
Medical DeviceFeb 4, 2026
Cardinal Health 200 Chest Drainage Units and Accessories: Product Code Description 1. recall — FDA Z-1203-2026
The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older. When used on infants, the CDU…
Class IIFDA: OngoingCardinal Health 200, LLC
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.