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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 501–520 of 1,000 recalls

Class ITerminated

Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02

CELLTRION USA INC

Returned test kits were erroneously shipped to customers. The kits are intended for Research Use Only (RUO). Additional RUO test kits were shipped to customers unlikely to use them for RUO purposes, and the firm provided a letter assuring distributors that RUO tests could be used for clinical diagnosis.

December 2, 2021 · DeviceView details →
Class IITerminated

Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic use in the quantitative determination of ¿2-microglobulin in human serum and plasma Siemens Material Number (SMN): 11097635

Siemens Healthcare Diagnostics, Inc.

¿2 Microglobulin (B2M) Reagent Lot 211446 Bias with Quality Control and Patient Sample Results. Positive bias on patient samples of up to +20.9% at a B2M concentration of approximately 1.5 mg/L and a negative bias on patient samples of up to -10.5% at a B2M concentration of approximately 15 mg/L

December 1, 2021 · Device
View details →
Class IITerminated

Hemashield Gold Knitted Bifurcated, 18 mm x 9 mm; reference number M002020851890

Maquet Cardiovascular, LLC

There is a probable mislabeling of product. A Hemashield Platinum Woven Double Velour Bifurcated Vasuclar Graft, SN 1259735369, 24 mm x 12 mm, REF Number M00202166241P0 is likely packaged inside of the carton instead of a Hemashield Gold Knitted Microvel Double Velour Bifurcated Vascular Graft; SN 1260004700; 18 mm x 9 mm; REF Number M002020851890 or a Hemashield Gold Knitted Microvel Double Velour Bifurcated Vascular Graft; SN 1259882880; 18 mm x 9 mm; Ref Number M002020851890.

December 1, 2021 · DeviceView details →
Class IITerminated

HARDY DIAGNOSTICS CatScreen, 25dsk/vial

MEDLINE INDUSTRIES, LP - Northfield

Product stored incorrectly in temperature controlled setting instead of refrigeration.

December 1, 2021 · DeviceView details →
Class IITerminated

Celltrion DiaTrust COVID-19 Ag Rapid Test, REF CT-P60 D-2 01. Contains 25 disposable test tubes with extraction buffer, 25 filter caps, 25 sterilized swabs per box.

CELLTRION USA INC

The European version of the DiaTrust COVID-19 Ag Rapid Test is not approved for marketing in the U.S. but was illegally distributed in the U.S. The packaging and labeling of the European test kit is different from the US test kit and is NOT authorized for distribution in the US.

December 1, 2021 · DeviceView details →
Class IITerminated

Premier Rotaclone, Rx only

MEDLINE INDUSTRIES, LP - Northfield

Product stored incorrectly in temperature controlled setting instead of refrigeration.

December 1, 2021 · DeviceView details →
Class IITerminated

Michels Transport Medium, 20ML Prefilled Cont

MEDLINE INDUSTRIES, LP - Northfield

Product stored incorrectly in temperature controlled setting instead of refrigeration.

December 1, 2021 · DeviceView details →
Class IITerminated

Regard, T AND A - Rogers, sterilized convenience kits

ROi CPS LLC

Kits lacks rubber latex warning label.

November 30, 2021 · DeviceView details →
Class IITerminated

Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107

Straumann USA LLC

Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 has an implant with measure of 3.5x13mm; and Carton Box (138.107- Easypack Helix GM Acqua has a 3.5x8mm implant instead of a 3.5x 13mm implant

November 30, 2021 · DeviceView details →
Class IITerminated

Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental implant Item 138.089

Straumann USA LLC

Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 has an implant with measure of 3.5x13mm; and Carton Box (138.107- Easypack Helix GM Acqua has a 3.5x8mm implant instead of a 3.5x 13mm implant

November 30, 2021 · DeviceView details →
Class IITerminated

Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605

MEDLINE INDUSTRIES, LP - Northfield

Affected product was shipped from the warehouse at room temperature instead of the required refrigerated environment.

November 30, 2021 · DeviceView details →
Class IITerminated

Proteus 235; Version: PTS-8 versions before PTS-8.7.2

Ion Beam Applications S.A.

Proton Therapy System (PTS) software can be started in the clinical environment (clinical user) while some processes are still running in the test environment (tcs user). Initiating the startup of the clinical processes in the environment is not prevented even if some processes of the test environment (tcs) are still running. It may lead to situations where the system is using test processes without notifying the clinical user. If the versions of the processes are different between both environments, this could have an impact on patient treatments.

November 29, 2021 · DeviceView details →
Class IITerminated

RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery User Manual/Treatment Planning User Manual: "RefleXion X1 Model: RXM1000"

Reflexion Medical, Inc.

Due to dose discrepancy when delivering a plan to a patient in a Non-HFS (Head First Supine) orientation specifically in Feet First Supine (FFS).

November 24, 2021 · DeviceView details →
Class IITerminated

BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use

Avanos Medical, Inc.

Product was distributed with incorrect expiration date.

November 22, 2021 · DeviceView details →
Class IITerminated

BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel Y- Adult, 16 French; Sterile; Single Use

Avanos Medical, Inc.

Product was distributed with incorrect expiration date.

November 22, 2021 · DeviceView details →
Class IITerminated

Electri-Cool II Portable Cold Therapy Unit, Model Number 767, Part Number 86193

Gentherm Medical, LLC

This recall has been initiated to provide a labeling update with revised instruction how to operate the unit with Cold Therapy pads.

November 22, 2021 · DeviceView details →
Class IITerminated

UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.

Uromedica Inc.

The U-channel sheaths may cause damage to ProACT implant devices when the devices are passed through the sheath during a ProACT implantation procedure.

November 22, 2021 · DeviceView details →
Class IITerminated

BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement for Multi-Access Port (MAP) Catheter; Sterile; Single Use

Avanos Medical, Inc.

Product was distributed with incorrect expiration date.

November 22, 2021 · DeviceView details →
Class ITerminated

WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6

Cardiovascular Systems Inc

Under certain circumstances, the WIRION filter assembly may become difficult to withdraw. Under such circumstances, alternative means may be necessary for withdrawal and the device may be prone to tearing or separating which may result in a risk for embolization.

November 22, 2021 · DeviceView details →
Class IITerminated

Philips Allura Xper FD series with Software Version Number: 2.1.x- intended for Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. Model Number: 722005, 722006, 722008, 722010, 722012, 722013, 722025, 722026, 722027, 722028.

Philips North America Llc

Set screws securing the two gliding rods of the Extra Monitors (called 7th and 8th monitor) mounted on the Monitor Ceiling Suspension (MCS) can come loose, the Extra monitors might disengage from the Mounting Ceiling Suspension structure and fall down, may lead to patient, user or service engineer harm that may require medical intervention.

November 19, 2021 · DeviceView details →
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