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[Recalled] Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103 — One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labe… | FDA 2022-07-22

FDA recall notice for Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103 (Corin Ltd). Reason: One MetaF

[Recalled] T-SPOT.TB REF TB.300 US — Due to equipment failure, affected products were stored at temperatures outside… | FDA 2022-07-07

FDA recall notice for T-SPOT.TB REF TB.300 US (OXFORD IMMUNOTEC LTD). Reason: Due to equipment failure, affected products were stored at temperatures outside….

[Recalled] T-Cell Xtend REF TTK.610 US — Due to equipment failure, affected products were stored at temperatures outside… | FDA 2022-07-07

FDA recall notice for T-Cell Xtend REF TTK.610 US (OXFORD IMMUNOTEC LTD). Reason: Due to equipment failure, affected products were stored at temperatures outsid

[Recalled] Medicina Reusable Oral syringe 2.5ml Code: OTH25 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina Reusable Oral syringe 2.5ml Code: OTH25 (Medicina Uk Ltd). Reason: Plunger component has been manufactured with an unapproved ma

[Recalled] Medicina Oral Tip Syringe 1ml Code: OT01 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina Oral Tip Syringe 1ml Code: OT01 (Medicina Uk Ltd). Reason: Plunger component has been manufactured with an unapproved material (

[Recalled] Medicina Reusable Oral syringe 5ml Code: OTH05 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina Reusable Oral syringe 5ml Code: OTH05 (Medicina Uk Ltd). Reason: Plunger component has been manufactured with an unapproved mate

[Recalled] Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 (Medicina Uk Ltd). Reason: Plunger component has been manufactured with an unap

[Recalled] Medicina Oral Tip Syringe 2.5ml Code: OT25 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina Oral Tip Syringe 2.5ml Code: OT25 (Medicina Uk Ltd). Reason: Plunger component has been manufactured with an unapproved material

[Recalled] Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD (Medicina Uk Ltd). Reason: Plunger component has been manufactured w

[Recalled] Medicina Oral Tip Syringe 0.5ml Code: OT005 — Plunger component has been manufactured with an unapproved material (Polyethyle… | FDA 2022-07-04

FDA recall notice for Medicina Oral Tip Syringe 0.5ml Code: OT005 (Medicina Uk Ltd). Reason: Plunger component has been manufactured with an unapproved materia

[Recalled] RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens: (1) Outer carton labeled as Rayner RayOne EMV US, REF RAO200E, SE: +19.00D, Sph: +19.00D; and (2) Inner p

FDA recall notice for RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens: (1) Outer carton

[Recalled] NanoSight NS300 — Product found to not comply to Class 1 Laser safety requirement | FDA 2022-04-07

FDA recall notice for NanoSight NS300 (MALVERN PANALYTICAL LTD). Reason: Product found to not comply to Class 1 Laser safety requirement. Issued 2022-04-07.

[Recalled] Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-2044 — Full screen error message may occur on patient monitors with a

FDA recall notice for Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video

[Recalled] VITROS Immunodiagnostic Products Troponin I ES Reagent Pack — Reagent packs could potentially contain incorrect wells, which will generate in… | FDA 2023-06-05

FDA recall notice for VITROS Immunodiagnostic Products Troponin I ES Reagent Pack (ORTHO-CLINICAL DIAGNOSTICS). Reason: Reagent packs could potentially contain

[Recalled] RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome. — DNAs used during the manufacture of two affected models were accide

FDA recall notice for RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequ

[Recalled] Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 — Defibrillator/pacemaker module (DPM) may encounter a problem causing communicat… | FDA 2023-05-08

FDA recall notice for Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 (Remote Diagnostic Technologies Ltd.). Reason: Defibrillator/pacemaker module

[Recalled] NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device — Device may experience malfunctions due to misalignment of the check valve in th… | FDA 2023-05-03

FDA recall notice for NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device (NOXBOX LTD). Reason: Device may experience malf

[Recalled] YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR — Optical Trocars sterility assurance can not be guaranteed | FDA 2023-03-28

FDA recall notice for YelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR (Surgical Innovations Ltd). Reason: Optical Trocars sterility assu

[Recalled] Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified personnel, for the attended or unattended monitoring of single or multiple vital signs in clinical and pre hos

FDA recall notice for Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified personnel, for the

[Recalled] NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL — One of the ball studs attaching a gas strut to the canopy may fail | FDA 2023-11-20

FDA recall notice for NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL (THO