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Medical Device Alert: Medical Devices Alert 2013/079 Hospira Administration sets

Ref: 2013/180 | Date: 18/11/2013

The Medicines and Healthcare products Regulatory Agency has issued an alert relating to the Hospira administration set Primary Plum set Clave secondary port.

Delisting: Product discontinuation Hewlett Packard Ink Cartridges.

Ref: 2013/179 | Date: 14/11/2013

We would like to inform customers that Hewlett Packard has given notification that 8 ink cartridges will no longer be available to purchase through NHS Supply chain.

Pricing Update: Price Reduction - Sendal Needlefree Connection Systems

Ref: 2013/177 | Date: 13/11/2013

From 1 October, Sendal have removed their Customer Commitment Discount for Needlefree Connection Systems and replaced it with lower sell prices against a range of their needlefree products.

Field Safety Notice: Field Safety Notice Infusion Pumps B. Braun Medical Ltd

Ref: 2013/176 | Date: 12/11/2013

B. Braun has issued a Field Safety Notice regarding the Perfusor Space pump when used in battery mode.

Delisting: Product Discontinuation - Dermagrip examination gloves

Ref: 2013/174 | Date: 11/11/2013

Fannin UK has taken the decision to discontinue the Dermagrip nitrile AF non sterile examination glove in all sizes.

Rationed Lines: Report for w/c 11 November 2013

Ref: 11/11/2013 | Date: 11/11/2013

Rationed lines report for w/c 11 November 2013

Medical Device Alert: MDA Alert 2013 078 Hospira Infusion Pumps

Ref: 2013/173 | Date: 07/11/2013

The MHRA have issued alert MDA/2013/078 on the 4th November 2013 regarding Plum and Gemstar Infusion Pumps.

Product Update: Lead time update - Zimmer Orthopaedic products

Ref: 2013/172 | Date: 05/11/2013

We would like to inform customers that Zimmer are experiencing delivery lead time issues on a number of their Orthopaedic products.

Recall: Product Recall Teleflex Cardiology Transradial Artery Access Kits

Ref: 2013/171 | Date: 05/11/2013

Teleflex Medical has issued a product recall due to the risk of the introducer needles packaged within their kits of Transradial Artery Access Kits becoming partially or fully occluded.

Recall: Product Recall - Hospira Administration Sets

Ref: 2013/170 | Date: 04/11/2013

Hospira UK Ltd has issued a product recall as three lot numbers of their Primary Plum sets have been manufactured with an incorrect fluid filter.

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