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  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 2541–2560 of 39,430 recalls

Class IOngoing

BIOGRAPH One (DE). Model Number: 11689172.

Siemens Medical Solutions USA, Inc

There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.

August 28, 2025 · DeviceView details →
Class IOngoing

MAGNETOM Verio Dot. Model Number: 10684333.

Siemens Medical Solutions USA, Inc

There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.

August 28, 2025 · DeviceView details →
Class IIOngoing

The AlignRT InBore system contains six Class 1 lasers which enables the system s cameras to track the patient s position and movement.

Vision RT Ltd

Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted from the Instructions for Use for the subject system as required by 21 CFR 1040,10(h), via conformance with recognized consensus standard IEC 60825-1 Ed. 3 (FDA Laser Notice 56).

August 27, 2025 · DeviceView details →
Class IIOngoing

Osstem Dental X-Ray System T2. Product Model Numbers T2-C and T2-CS.

OSSTEM Implant Co., Ltd.

Osstem Implant Co. Ltd, is voluntarily initiating a medical device correction involving the current labeling for this electronic product may be missing a required Certification Statement under 21 CFR Subchapter J (Radiological Health Regulations). Specifically, the following statement may have been omitted: Certification Statement: This electronic product complies with all applicable performance standards prescribed under 21 CFR Subchapter J, as enforced by the U.S. Food and Drug Administration at the date of manufacturing.

August 26, 2025 · DeviceView details →
Class IIOngoing

Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS.

OSSTEM Implant Co., Ltd.

Osstem Implant Co. Ltd, is voluntarily initiating a medical device correction involving the current labeling for this electronic product may be missing a required Certification Statement under 21 CFR Subchapter J (Radiological Health Regulations). Specifically, the following statement may have been omitted: Certification Statement: This electronic product complies with all applicable performance standards prescribed under 21 CFR Subchapter J, as enforced by the U.S. Food and Drug Administration at the date of manufacturing.

August 26, 2025 · DeviceView details →
Class IIOngoing

Osstem Dental X-Ray System T2Plus. Product Model Numbers T2-C-P and T2-CS-P.

OSSTEM Implant Co., Ltd.

Osstem Implant Co. Ltd, is voluntarily initiating a medical device correction involving the current labeling for this electronic product may be missing a required Certification Statement under 21 CFR Subchapter J (Radiological Health Regulations). Specifically, the following statement may have been omitted: Certification Statement: This electronic product complies with all applicable performance standards prescribed under 21 CFR Subchapter J, as enforced by the U.S. Food and Drug Administration at the date of manufacturing.

August 26, 2025 · DeviceView details →
Class IIOngoing

GORE ACUSEAL Vascular Graft, REF: ECH050020J, ECH050020W, ECH050050J, ECH050050W, ECH060010A, ECH060020A, ECH060020J, ECH060020W, ECH060040, ECH060040A, ECH060040W, ECH060050A, ECH060050J, ECH460045A, ECH460045J, ECH470045, ECH470045A; used with Instructions for Use.

W L Gore & Associates, Inc.

Reports of vascular graft delamination, which may lead to reduced access flow; cannulation difficulties; bleeding or bruising; and harms related to reintervention procedures, so Instructions for Use will be updated to modify existing warning to 1) further clarify techniques that may contribute to the risk of delamination, 2) Addition of delamination to device-related adverse event section.

August 26, 2025 · DeviceView details →
Class IIOngoing

Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is intended to serve as a substitute conduit for blood where bypass or replacement of occluded or diseased arterial segments is required or to establish a conduit for hemodialysis.

LeMaitre Vascular, Inc.

Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.

August 25, 2025 · DeviceView details →
Class IIOngoing

MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.

CooperVision, Inc.

One lot manufactured with an invalid sterilization cycle.

August 22, 2025 · DeviceView details →
Class IIOngoing

MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4

GE Medical Systems, LLC

If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable. This is visible as a damaged sheath or exposed wires. If a damaged Acquisition Trunk Cable is not recognized and removed from service, the cable can overheat with continued use.

August 22, 2025 · DeviceView details →
Class IIOngoing

Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.

CooperVision, Inc.

One lot manufactured with an invalid sterilization cycle.

August 22, 2025 · DeviceView details →
Class IIOngoing

Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description: Sonesta 6210 - Procedure table designed for full fluoroscopic imaging of the urinary tract during video Urodynamics procedures. Component: N/A

Sonesta Medical AB

Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.

August 22, 2025 · DeviceView details →
Class IIOngoing

Sofmed Breathables, (stenfilcon A) contact lens. Model Number: Softmed Breathables. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Blister packaged.

CooperVision, Inc.

One lot manufactured with an invalid sterilization cycle.

August 22, 2025 · DeviceView details →
Class IIOngoing

i-STAT EG6+ cartridge. List Number: 03P77-25.

Abbott Point Of Care Inc.

Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.

August 21, 2025 · DeviceView details →
Class IIOngoing

Frontier Devices, REF: 301.912S1, 12 mm Distraction Pin, 10 single packs , Rx Only, Sterile

Folsom Metal Products, Inc.

Labeling includes shelf life that has not been validated.

August 21, 2025 · DeviceView details →
Class IIOngoing

Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 5 single packs , Rx Only, Sterile

Folsom Metal Products, Inc.

Labeling includes shelf life that has not been validated.

August 21, 2025 · DeviceView details →
Class IIOngoing

i-STAT CG4+ cartridge (white). List Number: 03P85-25.

Abbott Point Of Care Inc.

Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.

August 21, 2025 · DeviceView details →
Class IOngoing

Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q

Medline Industries, LP

The kits contain certain lots of cannula products where the catheter may not retain its shape.

August 21, 2025 · DeviceView details →
Class IIOngoing

Frontier Devices, REF: 301.916S1, 16 mm Distraction Pin, 10 single packs , Rx Only, Sterile

Folsom Metal Products, Inc.

Labeling includes shelf life that has not been validated.

August 21, 2025 · DeviceView details →
Class IIOngoing

i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300

Abbott Point Of Care Inc.

Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.

August 21, 2025 · DeviceView details →
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