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[Recalled] Sterilize UVC Light Germicidal UVC LED Lamp Portable Home Handheld Disinfection — The product does not emit UV-C radiation | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for Sterilize UVC Light Germicidal UVC LED Lamp Portable Home Handheld Disinfection. Reason: The product does not emit UV-C radiati

[Recalled] SUBMERSIBLE FLORALYTE V — The battery compartment can be easily opened, leaving the button batteries acce… | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for SUBMERSIBLE FLORALYTE V (Kitosun Lights). Reason: The battery compartment can be easily opened, leaving the button batteries ac

[Recalled] Respirator — The product bears a CE marking but is not certified as protective equipment by… | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for Respirator (Elite). Reason: The product bears a CE marking but is not certified as protective equipment by…. Issued 2020-07-10.

[Recalled] UV Germicidal Lamp UVC with Ozone Bulb 8W 220v Timer Control — The product emits an unsafe amount of UV-C radiation (measured value: 2.1 W/m2) | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for UV Germicidal Lamp UVC with Ozone Bulb 8W 220v Timer Control. Reason: The product emits an unsafe amount of UV-C radiation (mea

[Recalled] LED Flood LIght Outdoor 50W — The electrical insulation is inadequate and the clearance/creepage distances be… | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for LED Flood LIght Outdoor 50W. Reason: The electrical insulation is inadequate and the clearance/creepage distances be…. Issued 2

[Recalled] Silicone Baby Teether Bear — The teether has protruding parts | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for Silicone Baby Teether Bear. Reason: The teether has protruding parts. Issued 2020-07-10.

[Recalled] UV Disinfection Light Home Room 36W UVC Ultraviolet Germicidal Sterilizing Lamps — The product does not emit UV-C radiation | EU Safety Gate 2020-07-10

EU Safety Gate recall notice for UV Disinfection Light Home Room 36W UVC Ultraviolet Germicidal Sterilizing Lamps. Reason: The product does not emit UV-C radiat

[Recalled] Transit, Transit Custom — The fuse for the electronic Run On Water Pump (ROWP) is inadequate and will not… | EU Safety Gate 2020-07-03

EU Safety Gate recall notice for Transit, Transit Custom (Ford). Reason: The fuse for the electronic Run On Water Pump (ROWP) is inadequate and will not…. Issue

[Recalled] Hair Clippers Men Professional Cordless Clippers — The product is advertised with a substandard adaptor for permanent use with ina… | EU Safety Gate 2020-07-03

EU Safety Gate recall notice for Hair Clippers Men Professional Cordless Clippers (Cheap4UK). Reason: The product is advertised with a substandard adaptor for p

[Recalled] Flyglobal — The product is advertised with a substandard adaptor for permanent use with ina… | EU Safety Gate 2020-07-03

EU Safety Gate recall notice for Flyglobal. Reason: The product is advertised with a substandard adaptor for permanent use with ina…. Issued 2020-07-03.

[Recalled] Professional Hair Clipper — The product is advertised with a substandard adaptor for permanent use with ina… | EU Safety Gate 2020-07-03

EU Safety Gate recall notice for Professional Hair Clipper (Surker). Reason: The product is advertised with a substandard adaptor for permanent use with ina…. I

[Recalled] Baby Cut of the Experts — The product is advertised with a substandard adaptor for permanent use with ina… | EU Safety Gate 2020-07-03

EU Safety Gate recall notice for Baby Cut of the Experts (Kemei). Reason: The product is advertised with a substandard adaptor for permanent use with ina…. Issu

[Recalled] NanoSight LM10 fitted with LM12 module. A laboratory instrument for determination of particle characteristics (e.g. size). — Product found to not comply to Class 1 Laser safety requirement | FDA 2022-02-28

FDA recall notice for NanoSight LM10 fitted with LM12 module. A laboratory instrument for determination of particle characteristics (e.g. size). (MALVERN PANAL

[Recalled] Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008 — Labelled with an incorrect expiry date on the outer label with an extended expi… | FDA 2022-02-14

FDA recall notice for Cytocell 8 Square Template Slides (Glass)- microscope slides Reference: PCN008 (Cytocell Ltd.). Reason: Labelled with an incorrect expir

[Recalled] TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome Catalog Number: LPH046-A — May show unexpected locus specific signals in addition to thos

FDA recall notice for TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome

[Recalled] Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503; YelloPort Elite Hasson Adaptor 10mm/EA10NH. For use in laparoscopic procedures. — Laparoscopic devices have a sterile symbol included on labels but devices

FDA recall notice for Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503; YelloPort Elite Hasson Adaptor 10mm/EA10NH. For use in laparosco

[Recalled] Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures. — Laparoscopic devices have a sterile symbol included on labels but devices are n… | FDA 2022-01-20

FDA recall notice for Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures. (Surgical Innovations Ltd). Reason: Lapar

[Recalled] Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024 — individual components have been labelled with incorrect colours | FDA 202

FDA recall notice for Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Num

[Recalled] Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S — Due to calibration curves producing a higher activity than routinely expected a… |

FDA recall notice for Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK0

[Recalled] Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy system — Base plate may detach from the main body of the treatment applicator | FDA 2021-08-27

FDA recall notice for Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy system (Xstrahl Limited). Reason: Base plate may det