
BEHA-AMPROBE Multimeters
The product has been recalled as it was discovered that an improperly rated fuse for CAT III 600V applications was installed in the affected products.
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The product has been recalled as it was discovered that an improperly rated fuse for CAT III 600V applications was installed in the affected products.

The product has been recalled as it has been identified that the button assembly on a limited number of 1.1” Omni Swivel Pulleys and associated variants may not be secure.

The product presents a high risk of choking due to easily detachable small parts.
On affected vehicles the position of the PTC Ground Wire may not be correctly anchored to the vehicle Body. This can potentially result in insulation being trapped between the wire and the body creating…
Additional to the batches included in the previous Class 4 Medicines Notification (reference EL(22)A/47), Martindale Pharma has made the MHRA aware that the GTIN in the 2D barcode and the printed variable data represents…
Affected motorcycles may have improper securing of the left-hand brake disc which may lead to its detachment from the front wheel assembly.

The product has been recalled as it has been identified that the mug could crack during use causing the hot contents to spill.

The product presents a serious risk of electric shock as it was found to be inadequately earthed.

The product presents a high risk of choking due to small parts generated following the tension test, and due to access to fibrous filling.
The fluid passage within the front brake master cylinder body may remain closed with the brake lever released due to improper position of the passage for adjusting the brake fluid pressure. This can lead…
The presence of Listeria monocytogenes in some batches of the products listed above.

The product presents a serious risk of fire as a manufacturing fault can lead to corrosion and the ability for the product to short circuit and ignite.

Product Safety Alert for angle grinder toothed saw blade attachments presenting a risk of serious injury or fatality. Consumers, local authority trading standards and businesses are asked to take specific action to cease use…
Following the conclusion of a review of post-marketing safety data by the MHRA, all pholcodine-containing medicines are being recalled and withdrawn from the UK as a precaution.
Affected vehicles have an engine control unit software that deviates from the local legal requirements.�
On affected vehicles the bolting of the 48V ground connection in the engine compartment might not be sufficiently tightened.
The vehicle identification number label may not have the correct maximum permissible laden mass printed on the VIN label.

The product presents a risk of choking as there is a risk that the poppers on the bags can become unsecure and detach.

The products present a risk of electric shock due to multiple issues such as failing the electrical strength test, containing counterfeit plugs and fuses, and poor internal build quality with access to live parts.

The product presents a serious chemical risk as it contains naphthalene which is a banned, carcinogenic substance.

The product presents a serious risk of choking as when drop tests and impact tests were performed, several of the eggs broke open releasing the small inner balls.
Rivets attaching certain ventilation windows to the main frame of the vehicle side windows may be subject to fatigue and fail.
On certain vehicles the front passenger airbag may not be securely bolted in place as intended.

Drugsrus Limited has informed the MHRA that the Patient Information Leaflet (PIL) packaged in specific batches of Clexane 10,000IU (100mg)/1 ml Syringes contains a typographical error in the leaflet.