June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pac
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
ConMed Corporation recalls ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units pe
Hazard: Potential for overpressure alerts.
June 24, 2026Medical DevicesFDA
Howmedica Osteonics Corp. recalls TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Hazard: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
June 24, 2026Medical DevicesFDA
Howmedica Osteonics Corp. recalls TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
Hazard: Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lot UZD9IB).
June 24, 2026Medical DevicesFDA
Accriva Diagnostics, Inc. recalls directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Hazard: Assayed Whole blood control contains labeling with incorrect performance range.
June 24, 2026Medical DevicesFDA
AMD Medicom Inc. recalls Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C
Hazard: Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.
June 24, 2026Medical DevicesFDA
AMD Medicom Inc. recalls Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.
Hazard: Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.
June 24, 2026Medical DevicesFDA
Abiomed, Inc. recalls Impella CP Set with SmartAssist. Product Codes: 1000080, 1000851, 0048-0014, 0048-0024-JP.
Hazard: Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.
June 24, 2026Medical DevicesFDA
Smith & Nephew, Inc. recalls TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816
Hazard: Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before implantation, an equivalent backup can be used, or a bent nail of the same size, which would require additional surgical steps to address soft tissue/bone preparation, which could lead to a surgical delay of greater than 30 minutes.
June 24, 2026Medical DevicesFDA
Medtronic Navigation, Inc.-Boxborough recalls Medtronic O-arm O2 Imaging System. Model Number: BI70002000.
Hazard: Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
June 24, 2026Medical DevicesFDA
Steris Corporation recalls ALYON Surgical Lighting System
Hazard: The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
June 24, 2026Medical DevicesFDA
Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System
Hazard: The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
June 24, 2026Medical DevicesFDA
Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System
Hazard: There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D C-SECTION DYNJ905094B C-SECTION
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE PICC DRSG TRAY DYNDC3291
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULA
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: PORT A CATH DYNJ906818A
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: ACL PACK DYNJ64161C ARTHROSCOPY PACK DYNJ47103D DYNJ67197G DYNJ85197A DYNJT4007
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX P
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT EB
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT DT17570
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: DAVINCI MAIN DYNJ908031D
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: WT LAVH PACK DYNJ46609F
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
June 24, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C
Hazard: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.