MHRA Class 2 Medicines Recall: KidNaps (Melatonin) 1mg in 1ml Oral Solution (Sterling Pharmaceuticals Ltd)

Drug alert number: EL(26)A/09

Date issued: 23 February 2026

Sterling Pharmaceuticals Ltd and Veriton Pharma Ltd are recalling all batches of KidNaps (Melatonin) 1mg in 1ml Oral Solution due to out of specification stability results.

DMRC reference number: DMRC-38487919

Company name: Sterling Pharmaceuticals Ltd (specials manufacturer MS 32515)

Medicine Details

KidNaps (Melatonin) 1mg in 1ml Oral Solution

Licence: MS 32515

Active ingredient: melatonin

GTIN: 5060191450331

Affected Lot Batch Numbers:

Batch No. Expiry Date Pack Size First Distributed
1743 Mar 2026 200ml 05/11/2024
1744 Mar 2026 200ml 12/11/2024
1787 Jun 2026 200ml 04/02/2025
1788 Jun 2026 200ml 21/02/2025
1852 Dec 2026 200ml 22/04/2025
1853 Dec 2026 200ml 27/06/2025
1955 Jun 2027 200ml 02/09/2025
1956 Jun 2027 200ml 05/11/2025
1992 Sep 2027 200ml 14/12/2025
1993 Sep 2027 200ml 05/02/2026

Background

Sterling Pharmaceuticals Ltd (specials manufacturer MS 32515) and Veriton Pharma Ltd are recalling all batches of KidNaps (Melatonin) 1mg in 1ml Oral Solution within expiry due to confirmed out of specification results from annual stability testing relating to product appearance and total impurities.

Advice for Healthcare Professionals

Stop supplying the above batches immediately. Quarantine all stock and return it to your supplier using your supplier’s approved process.

View the full alert here.

Advice for Patients

No action is required by patients, the recall is at the wholesaler and pharmacy level.

The recall is being undertaken out of an abundance of caution, patients using this medication may continue to do so. No adverse reactions have been reported from patients using this product. Patients or carers who have concerns about their medication should speak to their healthcare professional in the first instance.

Patients who experience adverse reactions or have any questions about the medication, should seek medical attention. Any suspected adverse reactions should also be reported via the MHRA Yellow Card scheme on https://yellowcard.mhra.gov.uk/

Additional information

For medical information enquiries on this product, email centralmedicalinformation@veritonpharma.com or telephone +44 (0)1932 690325.

For stock control enquiries, email orders@veritonpharma.com or telephone +44 (0)1932 690325.

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