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Articles about: United Kingdom

686 articles — Page 19 of 35

[Recalled] Compact Swivel Range — The swivel has been assembled incorrectly and the two sides of the swivel could… | EU Safety Gate 2019-11-29

EU Safety Gate recall notice for Compact Swivel Range (DMM). Reason: The swivel has been assembled incorrectly and the two sides of the swivel could…. Issued 20

[Recalled] AC Electrical Adaptor — The electrical strength of the product is inadequate | EU Safety Gate 2019-11-29

EU Safety Gate recall notice for AC Electrical Adaptor (Joylit). Reason: The electrical strength of the product is inadequate. Issued 2019-11-29.

[Recalled] Ranger Diesel — The fuel line is not sufficiently protected | EU Safety Gate 2019-11-29

EU Safety Gate recall notice for Ranger Diesel (Polaris). Reason: The fuel line is not sufficiently protected. Issued 2019-11-29.

[Recalled] BriteBlade Pro Single-Use Fiber Optic Mac 3, CE01120, Do Not Re-use, Rx Only, REF 040-713U, Sterile EO, Qty 10, (01)15055788723001 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the voc

FDA recall notice for BriteBlade Pro Single-Use Fiber Optic Mac 3, CE01120, Do Not Re-use, Rx Only, REF 040-713U, Sterile EO, Qty 10, (01)15055788723001 The

[Recalled] BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2, CE 0120, Do not Re-use, Rx Only, REF: 040-342U, Sterile EO, Qty 10, UDI: (01)15055788724053(17)230901(10)181002320 — The firm has received reports that the spring/w

FDA recall notice for BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2, CE 0120, Do not Re-use, Rx Only, REF: 040-342U, Sterile EO, Qty 10, UDI:

[Recalled] BriteBlade Pro Single-se Fiber Optic Miller 2, CE 0120, Do not Re-use, Rx Only, REF, 040-722U, Sterile EO, Qty 10, (01) 15055788722783 The device is intended for direct vision laryngoscopy to obtain an illuminated view of the

FDA recall notice for BriteBlade Pro Single-se Fiber Optic Miller 2, CE 0120, Do not Re-use, Rx Only, REF, 040-722U, Sterile EO, Qty 10, (01) 15055788722783

[Recalled] BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile EO, Qty 10, (01)15055788724138(17)230801(10)180900072 The device is intended for direct vision laryngoscopy

FDA recall notice for BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3, CE 0120, Do not Re-use, Rx Only, REF, 040-333U, Sterile EO, Qty 10, (01)1505

[Recalled] Ranger XP 1000 — The fuel line is not sufficiently protected | EU Safety Gate 2019-11-22

EU Safety Gate recall notice for Ranger XP 1000 (Polaris). Reason: The fuel line is not sufficiently protected. Issued 2019-11-22.

[Recalled] FreshpackPro-QH — The poor quality of the internal build can easily lead to breakdown at low volt… | EU Safety Gate 2019-11-22

EU Safety Gate recall notice for FreshpackPro-QH (Xin Boa long). Reason: The poor quality of the internal build can easily lead to breakdown at low volt…. Issue

[Recalled] Crystal Ceiling Light — The internal build and the fuse are inadequate, causing the product to break do… | EU Safety Gate 2019-11-22

EU Safety Gate recall notice for Crystal Ceiling Light (Paths). Reason: The internal build and the fuse are inadequate, causing the product to break do…. Issued

[Recalled] Slingshot S / SL / SLR / GT — Under certain conditions, the capability of the battery fuse block terminals mi… | EU Safety Gate 2019-11-22

EU Safety Gate recall notice for Slingshot S / SL / SLR / GT (Polaris). Reason: Under certain conditions, the capability of the battery fuse block terminals mi…

[Recalled] Magnetic Building Blocks — The product contains small loose parts and a plastic packaging that can become… | EU Safety Gate 2019-11-08

EU Safety Gate recall notice for Magnetic Building Blocks (Jasonwell). Reason: The product contains small loose parts and a plastic packaging that can become….

[Recalled] Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI: 05051700018319 — It has been identified that the rheumatoid factor (RF) calibrator values over r… | FDA 2019-11-06

FDA recall notice for Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Product code: LK151.S.A. , UDI: 05051700018319 (The Binding Si

[Recalled] Ranger, Everest — The ammonium nitrate propellant used in the airbag inflator may experience a ma… | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for Ranger, Everest (Ford). Reason: The ammonium nitrate propellant used in the airbag inflator may experience a ma…. Issued 2019-1

[Recalled] Swing — The product is incorrectly labelled as being suitable for small children. The c… | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for Swing (Kingsport). Reason: The product is incorrectly labelled as being suitable for small children. The c…. Issued 2019-11-01.

[Recalled] Yun fan 100 x three coloured balloons — The amount of nitrosamines released by the balloons is too high (measured value… | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for Yun fan 100 x three coloured balloons (Unknown). Reason: The amount of nitrosamines released by the balloons is too high (measu

[Recalled] M3W — The weld fillet between the pedal mount and arm may be missing | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for M3W (Morgan). Reason: The weld fillet between the pedal mount and arm may be missing. Issued 2019-11-01.

[Recalled] Electronical Mosquito Killer — The internal high tension connections are done by wire twisting | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for Electronical Mosquito Killer (Unknown). Reason: The internal high tension connections are done by wire twisting. Issued 2019-11

[Recalled] Brake master cylinder — The secondary seal may fall within the brake master cylinder | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for Brake master cylinder (Liberty Vehicle Technologies). Reason: The secondary seal may fall within the brake master cylinder. Iss

[Recalled] Ranger P150 — The ammonium nitrate propellant used in the airbag inflator may experience a ma… | EU Safety Gate 2019-11-01

EU Safety Gate recall notice for Ranger P150 (Ford). Reason: The ammonium nitrate propellant used in the airbag inflator may experience a ma…. Issued 2019-11-01