Latest recalls — page 35

Browse the most recent U.S. safety recalls in our connected official government data.

3,525 recalls in our current data. Showing 3,401–3,500, newest first.

FDA Class II · Medical device · April 29, 2026

Flamingo Funnel Large recall — SurgiSmoke Solutions

Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.

Company / brand: SurgiSmoke Solutions recalls

Official ID Z-1926-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Flamingo Funnel Medium recall — SurgiSmoke Solutions

Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.

Company / brand: SurgiSmoke Solutions recalls

Official ID Z-1925-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Flamingo Funnel Small recall — SurgiSmoke Solutions

Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.

Company / brand: SurgiSmoke Solutions recalls

Official ID Z-1924-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Oxoid Agglutinating Sera recall — Remel Europe Ltd.

Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O seroty…

Company / brand: Remel Europe recalls

Official ID Z-1923-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Access Total T4 Calibrator recall — Beckman Coulter, Inc.

Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product specifications. A fal…

Company / brand: Beckman Coulter recalls

Official ID Z-1922-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Custom Convenience Kits Pre Op Kit - NS recall — Windstone Medical Packaging, Inc.

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …

Company / brand: Windstone Medical Packaging recalls

Official ID Z-1921-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Custom Convenience Kits Pre Op Kit - NS recall — Windstone Medical Packaging, Inc.

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …

Company / brand: Windstone Medical Packaging recalls

Official ID Z-1920-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Custom Convenience Kits Pre Op Kit - NS recall — Windstone Medical Packaging, Inc.

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets …

Company / brand: Windstone Medical Packaging recalls

Official ID Z-1919-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Rover Mobile X-ray System Model/Catalog Number recall — Micro-X Ltd.

X-Ray generator may malfunction resulting in the X-Ray being inoperable.

Company / brand: Micro-X recalls

Official ID Z-1918-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7 recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1917-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

MAC" Two-Lumen Central Venous Access Kit for use with 7 recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1916-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1915-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

ARROW recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1914-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

FLEXTIP PLUS EPIDURAL CATHETER recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1913-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

PERCUTANEOUS SHEATH INTRODUCER with 7 recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1912-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1911-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code recall — ARROW INTERNATIONAL, LLC

Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

Company / brand: ARROW INTERNATIONAL recalls

Official ID Z-1910-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1909-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1908-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1907-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1906-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1905-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1904-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

XXX

Company / brand: Olympus of the Americas recalls

Official ID Z-1903-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1902-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1901-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1900-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1899-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

OER-ELITE Endoscope Reprocessor Connecting Tubes recall — Olympus Corporation of the Americas

Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Company / brand: Olympus of the Americas recalls

Official ID Z-1898-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90- recall — XTANT Medical Holdings, Inc

Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.

Company / brand: XTANT Medical Holdings recalls

Official ID Z-1897-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6 recall — Davol, Inc.

Potential for product to contain foreign matter, confirmed to be inspect fragments.

Company / brand: Davol recalls

Official ID Z-1896-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

LeadCare Ultra Blood Lead Test Kit recall — Magellan Diagnostics, Inc.

Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test S…

Company / brand: Magellan Diagnostics recalls

Official ID Z-1895-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

LeadCare¿ Plus Blood Lead Test Kit recall — Magellan Diagnostics, Inc.

Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test S…

Company / brand: Magellan Diagnostics recalls

Official ID Z-1894-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

(1)(2) LeadCare¿ II Blood Lead Test Kit recall — Magellan Diagnostics, Inc.

Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test S…

Company / brand: Magellan Diagnostics recalls

Official ID Z-1893-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ENS recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1892-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ART recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1891-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADD recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1890-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes E P recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1889-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ART recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1888-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EXT recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1887-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EYE recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1886-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1885-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANG recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1884-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Med recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1883-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes FAC recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1882-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BAR recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1881-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes MIN recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1880-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIO recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1879-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAV recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1878-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADU recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1877-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUD recall — Medline Industries, LP

Unapproved design changes to the products outside of the 510(k) clearance.

Company / brand: Medline Industries recalls

Official ID Z-1876-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

AccuVu Angiographic Catheter recall — Angiodynamics, Inc.

The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.

Latest recalls — page 35

Official sources