Medical DeviceJun 24, 2026
ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm recall — FDA Z-2467-2026
Potential for overpressure alerts.
Class IIFDA: OngoingConMed Corporation
June 2026 recalls — page 3
These records include useful source details for the selected month.
Medical DeviceJun 24, 2026
MEDLINE Pre-connected Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr recall — FDA Z-2481-2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish,…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
BD SWITZERLAND SARL BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD recall — FDA Z-2514-2026
Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some…
Class IIFDA: OngoingBD SWITZERLAND SARL
Medical DeviceJun 24, 2026
Medline convenience kits: BASIC DYNJ905869G BASIC PACK DYNJ68484B BIB GENERAL LAPAROSCOPY PA recall — FDA Z-2424-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
GE Medical Systems Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 recall — FDA Z-2477-2026
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport,…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJun 24, 2026
MEDLINE Urethral Catheterization Tray, Red Rubber Latex, Medline Product Number/SKU (REF) recall — FDA Z-2480-2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish,…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
ARROW INTERNATIONAL Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 recall — FDA Z-2368-2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of…
Class IFDA: OngoingARROW INTERNATIONAL, LLC
Medical DeviceJun 24, 2026
Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D C-SECTION recall — FDA Z-2446-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
MEDLINE Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product recall — FDA Z-2482-2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish,…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR recall — FDA Z-2509-2026
Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses.
Class IIFDA: OngoingStaar Surgical AG
Medical DeviceJun 24, 2026
ARROW INTERNATIONAL Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN recall — FDA Z-2396-2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of…
Class IFDA: OngoingARROW INTERNATIONAL, LLC
Medical DeviceJun 24, 2026
Howmedica Osteonics TRI TS BASEPLATE SIZE 4 recall — FDA Z-2462-2026
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…
Class IIFDA: OngoingHowmedica Osteonics Corp.
Medical DeviceJun 24, 2026
Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG recall — FDA Z-2419-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
MEDLINE Urethral Catheter, Red Rubber Latex, Medline Product Number/SKU (REF), French sizes recall — FDA Z-2479-2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish,…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
Datex-Ohmeda Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers recall — FDA Z-2359-2026
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the…
Class IFDA: OngoingDatex-Ohmeda Inc
Medical DeviceJun 24, 2026
Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ENDO BREAST recall — FDA Z-2423-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L recall — FDA Z-2447-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
ARROW INTERNATIONAL Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP recall — FDA Z-2393-2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of…
Class IFDA: OngoingARROW INTERNATIONAL, LLC
Medical DeviceJun 24, 2026
Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK recall — FDA Z-2444-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
HeartMate HM 11V Li-ion Backup Battery, ABT recall — FDA Z-2520-2026
Due to 11 volt Backup Battery failures.
Class IIFDA: OngoingThoratec LLC
Medical DeviceJun 24, 2026
ARROW INTERNATIONAL Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH recall — FDA Z-2365-2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of…
Class IFDA: OngoingARROW INTERNATIONAL, LLC
Medical DeviceJun 24, 2026
Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE PICC DRSG recall — FDA Z-2445-2026
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK, Medline Kit Number/SKU recall — FDA Z-2504-2026
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish,…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceJun 24, 2026
ARROW INTERNATIONAL Description/REF: ACCESS TRAY/ASK-04001-SUH-S recall — FDA Z-2364-2026
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of…
Class IFDA: OngoingARROW INTERNATIONAL, 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.