February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF, Kit SKU DYNJ20028L; 2) NEURO MINOR
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880; 2) ADULT CVC
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY, Kit SKU ACC010270A; 2) DRAWER 2, Kit SKU
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R; 2) PLAST
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDO
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O; 2) HEAD AND NECK CDS-
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L; 2) BREAST
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMA
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF, Kit SKU DYNJ64837C; 2) LOOP R
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713
Hazard: 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 MASTISOL Liquid Adhesive.
February 4, 2026Medical DevicesFDA
NIPRO Technical Services, Inc. recalls Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conducti
Hazard: due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls PREGNANCY TEST 24CT
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W B
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS T
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CO
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
GOLD STAR DISTRIBUTION INC recalls Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
Hazard: Potential exposure of rodents and rodent activity in the distribution center.
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000V, interventional fluoroscopic x-ray system
Hazard: 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 become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000H, interventional fluoroscopic x-ray system
Hazard: 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 become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000F, interventional fluoroscopic x-ray system
Hazard: 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 become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Canon Medical System, USA, INC. recalls Alphenix INFX-8000C, interventional fluoroscopic x-ray system
Hazard: 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 become loose. As a result, ceiling lateral movement may no longer be possible, abnormal noise may be generated from the suspension system and a sensor error may be displayed
February 4, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Ve
Hazard: 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.
February 4, 2026Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Ve
Hazard: 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.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls AlternatiV+ Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls AlternatiV+ Max Knotless Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Push-In Suture Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Knotless Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Dual Thread Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Genesis Screw-In Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.
February 4, 2026Medical DevicesFDA
Aju Pharm Co., Ltd. recalls Fixone Biocomposite Anchor
Hazard: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.