227 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
Hanger-Bar 2P 45cm
FDA Recall
Open, Classified
·Human Care USA, Inc.·Product code FSA·November 1, 2021
Hanger-Bar 2P 45cm
FDA Recall
Open, Classified
·Human Care USA, Inc.·Product code FSA·November 1, 2021
Sechrist Low Profile Wheeled Stretcher, Model No. 21762-110-33H, 21762-110-36H, 21762-110-41H, 21762-135-33HJ, 21762-010-36H, 21762-010-41H, 21762-111-36H.
FDA Recall
Terminated
·Sechrist Industries Inc·Product code FPO·June 1, 2015
Alinity m System, Part Number: 08N53-002
FDA Recall
Open, Classified
·Abbott Molecular, Inc.·Product code OOI·March 20, 2024
VIASYS Healthcare Disposable Bar Electrodes. Re-order No. 019-435600. Single Use only. Manufactured in the U.S.A. for VIASYS Healthcare, 5225 Verona Road, Bldg 2, Madison, WI USA 53711-4495..Each box contains 10 pouches of Bar Electrodes and each pouch contains 10 electrodes
FDA Recall
Terminated
·Nicolet Biomedical Div of Viasys Healthcare·Product code GXZ·April 28, 2006
Liko Universal Sling Bar 450 R2R Product NUmber: 3156095
FDA Recall
Terminated
·Liko, Inc.·Product code FRW·June 13, 2007
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
FDA Recall
Open, Classified
·Intrinsic Therapeutics, Inc.·Product code LXH·July 25, 2024
Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/ "Alere" iCup Dx 10 Drug Detection + Adulteration AMP/BAR/BZO/COC/MET/MDMA/MTD/MOP/OXY/THC Bl, Cr, Ni, pH, SG", I-DXA-13B/"Alere" iCup DX Drug Screen Cup 13 Drug Detection + Adulteration AMP/BAR/BZO/BUPG/COC/MET/MDMA/MTD/MOP/OXY/PCP/THC/TCA Bl, Cr, Ni, pH, SG", I-DXA-1127-023-N "Alere" iCup Dx Drugs of Abuse Test (COC/THC)+(MET1000/OPI2000)+(MTD/TCA)+ (OXY/MDMA)+(PCP/AMP)+BAR+BZO With Cr, Ni, pH, Bl, S.G."
FDA Recall
Terminated
·Ameditech Inc·Product code DIO·August 18, 2020
Liko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085
FDA Recall
Terminated
·Liko, Inc.·Product code FRW·June 13, 2007
Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A.
FDA Recall
Terminated
·Hill-Rom, Inc.·Product code KMM·November 14, 2003
Electrode, Barrel Bar, 24FR (27050NX/6). Resectoscope accessories (ie. electrode, cutting loops and cold knives).
FDA Recall
Terminated
·Karl Storz Endoscopy America Inc·Product code FJL·June 1, 2009
DrugCheck 8 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP Product Code 60800
FDA Recall
Terminated
·Drug Free Enterprises Inc·Product code DIO·March 20, 2003
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
FDA Recall
Open, Classified
·Moller Vital Hadelandsvegen 2·Product code FSA·February 4, 2019
DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/TCA Product Code 60900
FDA Recall
Terminated
·Drug Free Enterprises Inc·Product code DIO·March 20, 2003
DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/MTD Product Code 60925
FDA Recall
Terminated
·Drug Free Enterprises Inc·Product code DIO·March 20, 2003
Zimmer Freestanding Patient Helper for Hill-Rom Totalcare beds; Zimmer Inc., Warsaw, IN; Prod. Nos. 00-2700-965-00 and 00-0965-001-00. The product is a L shaped bar that is used with hospital beds set up for traction. The bar allows mounting of a trapeze to help the patient pull themselves up when in the hospital bed.
FDA Recall
Terminated
·Zimmer Inc.·Product code IKX·July 7, 2008
Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
FDA Recall
Terminated
·Synthes, Inc.·Product code HWB·March 19, 2018
Stryker, REF: 0250070460, 5.0 mm x 32 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 07613327051971 These products are distributed with the following sheath/probe: 0250070441-PKG, StrykeFlow Electrocautery Probe, Spatula Tip 5MM 0250070442-PKG, StrykeFlow Electrocautery Probe, J Tip, 5MM 0250070443-PKG, StrykeFlow Electrocautery Probe, L Tip, 5MM 0250070444-PKG, StrykeFlow Electrocautery Probe, Ball Tip, 5MM 0250070445-PKG, StrykeFlow Electrocautery Probe, Needle Tip 5MM 0250070446-PKG, StrykeFlow Electrocautery Probe, Spoon Tip, 5MM
FDA Recall
Terminated
·Stryker Corporation·Product code GEI·September 12, 2019
Stryker, REF: 0250070450, 5.0 mm x 45 cm, Strykeprobe, Outer Sheath Replacement, RX Only, Non-Sterile, CE, UDI: (01) 07613327051926 This products was distributed with the following sheath/probe: 0250070451-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, Spatula-Tip, 0250070452-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, J-TIP, 0250070453-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, L-TIP, 0250070455-PKG, 5MM X 45CM StrykeProbe Electrosurgical Probe, Needle Tip
FDA Recall
Terminated
·Stryker Corporation·Product code GEI·September 12, 2019
Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
FDA Recall
Open, Classified
·MEDLINE INDUSTRIES, LP Northfield·Product code QTC·March 5, 2024