41 results · 14ms · Sources: EU EUDAMED, US FDA

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CoolCurve+ ZELTIQ Vacuum Applicator REF BRZ-AP1-064-000

FDA Recall
Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

CoolFit ZELTIQ Vacuum Applicator REF BRZ-AP1-066-000

FDA Recall
Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

CoolCurve ZELTIQ Vaccum Applicator REF BRZ-AP1-062-000

FDA Recall
Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

FDA Recall
Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

CoolCore ZELTIQ Vacuum Applicator REF BRZ-AP1-063-000

FDA Recall
Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)

FDA Recall
Open, Classified ·Product code OEZ·May 4, 2026

Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)

FDA Recall
Open, Classified ·Given Imaging Ltd. New Industrial Park·Product code FFT·June 3, 2025

Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL KIT, REF DYNJRA2210; c) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046; d) PARACERVICAL/PUDENDAL BLK KIT, REF DYNJRA9046H; Medical procedure convenience tray

FDA Recall
Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OJH·March 1, 2024

STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.

FDA Recall
Open, Classified ·Product code JIN·October 2, 2023

NxStage PureFlow-B Solution, Premixed Dialysate for Hemodialysis, Device Catalog Numbers RFP-400, RFP-401, RFP-402, RFP-403, RFP-404, RFP-405, RFP-406, RFP-453, RFP-454, RFP-456

FDA Recall
Open, Classified ·NxStage Medical Inc·Product code KPO·May 14, 2024

SENTIERO Screening2, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S2

FDA Recall
Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023

SENTIERO SCREENING, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-S

FDA Recall
Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023

SENTIERO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098

FDA Recall
Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023

AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP

FDA Recall
Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code EWO·September 26, 2023

MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)

FDA Recall
Open, Classified ·PATH Landsberger Str. 65 Germering Germany·Product code GWJ·November 6, 2025

HME for Tracheostomized Patients, Item Code 353S13046 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.

FDA Recall
Open, Classified ·Product code CAH·April 29, 2021

Anesthesia circuit kit; CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230

FDA Recall
Open, Classified ·Product code CAH·October 10, 2025

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

FDA Recall
Open, Classified ·Draeger, Inc.·Product code CAH·June 16, 2025

CircuitGuard Bacterial/Viral Filter with Elbow (Model/Catalogue number: SK200FPE / 7056)

FDA Recall
Open, Classified ·Kung Shin Plastics Co. Ltd. 65-2 Erh Chia Road Ying Kuo Town Taipei Hsien Taiwan·Product code CAH·January 9, 2025

Mechanical Filter with Connector Small, Tethered Cap, Item Code 351/5979 - Product Usage: indicated for single use on anesthetized patients and respiratory care patients who require a breathing circuit with ISO standard 15mm or 22 mm connectors.

FDA Recall
Open, Classified ·Product code CAH·April 29, 2021