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Important Customer Notices

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Recall: Renal Replacement Therapies Asahi Kasei

Ref: 2016/108 | Date: 23/06/2016

Asahi Kasei has appointed a distributor for their renal products

Product Update: Baxter Healthcare Ltd FSB835 Pump Administration Set: Return to Normal Supply

Ref: 2016/106 | Date: 20/06/2016

Supply of the following Baxter Healthcare product has returned to normal, allowing for customer ordering to be re-established from Monday 27th June 2016

Product Update: Standard Endotracheal tube uncuffed with Murphy eye

Ref: 2016/100 | Date: 17/06/2016

The 111 range of standard endotracheal tubes have been upgraded by the manufacturer Medtronic

Product Update: Maquet Limited – Product Removal

Ref: 2016/095 | Date: 17/06/2016

Maquet Medical are not accepting any orders for shipping products listed on the attached sheet unless the purchaser has completed a Certificate of Medical Necessity

Product Update: Vygon Supply Issues FTR221, FTR222, FTR223 and FTM036

Ref: 2016/103 | Date: 17/06/2016

Vygon UK Ltd is experiencing major supply issues on some of their products, due to a component issue.

Product Update: ENFit connector update - NPC’s

Ref: 2016/105 | Date: 17/06/2016

A new global enteral feeding device connector design (named ENFit) is in the process of being implemented in a two phase process nationwide

Delisting: bioMérieux UK Ltd delist alternative

Ref: 2016/104 | Date: 17/06/2016

KFK381 and KFK382 delisted as supplier did not tender for new Blood Collection Systems and Blood Lancets Framework

Field Safety Notice: Aspen Medical Field Safety Notice Sorbsan Dressings

Ref: 2016/094 | Date: 15/06/2016

Aspen Medical has issued a field safety notice affecting a range of Sorbsan dressings following discovery of the application of incorrect expiry dates.

Field Safety Notice: Field Safety Notice Metalline products

Ref: 2016/102 | Date: 14/06/2016

Activa Healthcare has issued a precautionary field safety notice following discovery during QC checks that needles used in the manufacturing process were detected on the back facing of the product.

Delisting: Ethicon Physiomesh Flexible Composite Mesh withdrawal from market

Ref: 2016/097 | Date: 13/06/2016

Following the precautionary recall of their Physiomesh flexible composite mesh range by Ethicon, see ICN093, these products have been withdrawn from the market.

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