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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 1661–1680 of 39,430 recalls

Class IOngoing

GE Healthcare Carestation anesthesia system Power Management Board (PMB) Field Replaceable Unit (FRU), 2076139-001-S

GE Medical Systems China Co., Ltd.

Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure. Anesthesia systems only operate on battery power in a rare event that AC mains power is lost and there is no continuous backup emergency power. If AC power is interrupted, the system will not automatically switch over to the battery supply mode and will reboot. If this issue occurs, a temporary disruption of mechanical ventilation, manual ventilation, and volatile agent delivery may occur. Following the reboot, the system will not return to the previous ventilation settings.

November 14, 2025 · DeviceView details →
Class IIOngoing

Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones.

Olympus Corporation of the Americas

Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.

November 14, 2025 · DeviceView details →
Class IIOngoing

Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20

Abbott Laboratories

Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues found in the Alinity ci-series System software versions 3.6.1. and lower that could lead to erroneous results for multiple analytes. The issue was identified by Abbott during the internal testing of complaint investigations.

November 13, 2025 · DeviceView details →
Class IIOngoing

KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K

Microbiologics Inc

Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.

November 13, 2025 · DeviceView details →
Class IIOngoing

InPen App, Model/CFN Number: MMT-8061 (Android Users)

Medtronic MiniMed, Inc.

When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow notifications to override phone settings when on mute/Do Not Disturb, and previously set up override permission is deleted, so audible and vibratory notifications not received, which may lead to delayed insulin therapy, hyperglycemia.

November 13, 2025 · DeviceView details →
Class IIOngoing

SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000

Medline Industries, LP

The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.

November 13, 2025 · DeviceView details →
Class IIOngoing

FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048

Medline Industries, LP

The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.

November 13, 2025 · DeviceView details →
Class IIOngoing

The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diodes (LEDs) as well as an electronics control unit for the LEDs which includes its own battery power supply. The measured LED positions can be used in one of three different modes of operation: Patient tracking, Registration using surface matching, and Automatic intra-operative mask registration.

Howmedica Osteonics Corp.

When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.

November 12, 2025 · DeviceView details →
Class IIOngoing

ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T ChemoPlus Full Coverage Gown, Closed Back, Regular/Medium, Medium Blue, Non-sterile; CT5503T ChemoPlus Full Coverage Gown, Closed Back, Large, Medium Blue, Non-sterile; CT5504T ChemoPlus Full Coverage Gown, Closed Back, Extra Large, Medium Blue, Non-sterile; CT5505T ChemoPlus Full Coverage Gown, Closed Back, Extra Extra Large, Medium Blue, Non-sterile; DP5001GT ChemoPlus Full Coverage Gown, Open Back, Large, medium Blue, Non- sterile; DP5002GT ChemoPlus Full Coverage Gown, Open Back, Extra Large, medium Blue, Non-sterile; DP5003GT ChemoPlus Full Coverage Gown, Open Back, Medium, medium Blue, Non-sterile; DP5004GT ChemoPlus Full Coverage Gown, Open Back, Extra Extra Large, medium Blue, Non-sterile; CT5500TS ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Sterile; CT5502TS ChemoPlus Full Coverage Gown, Closed Back, Regular/Medium, Medium Blue, Non-sterile; CT5503TS ChemoPlus Full Coverage Gown, Closed Back, Large, Medium Blue, Sterile; CT5504TS ChemoPlus Full Coverage Gown, Closed Back, Extra Large, Medium Blue, Sterile; CT5505TS ChemoPlus Full Coverage Gown, Closed Back, Extra Extra Large, Medium Blue, Sterile;

Cardinal Health 200, LLC

Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.

November 12, 2025 · DeviceView details →
Class IIOngoing

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

Remel, Inc

Products may contain contamination, which may result in a darker or brown media color.

November 12, 2025 · DeviceView details →
Class IIOngoing

Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
Class IIOngoing

Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.

Olympus Corporation of the Americas

Complaints of the ceramic tip of the resection sheath breaking have been received.

November 11, 2025 · DeviceView details →
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