Class 2 Medicines : Norgine Pharmaceuticals Limited, Pedmarqsi 80
OFFICIAL-SOURCE RECALL · UNITED KINGDOM
UPDATE: Class 4 Medicines Defect Notification: Relonchem Limited Recall: Relonchem Limited have informed the
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryUnited KingdomPublishedJune 30, 2026Last updatedJuly 7, 2026Official source last checkedSeptember 9, 2026 at 1:48 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- UPDATE: Class 4 Medicines Defect Notification: Relonchem Limited, Gabapentin Relonchem 50mg/ml Oral Solution, EL(26)A/31
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Relonchem Limited have informed the MHRA that particles have been observed inside some bottles of Gabapentin Relonchem Oral Solution, identified through a customer complaint.
Hazard
Relonchem Limited have informed the MHRA that particles have been observed inside some bottles of Gabapentin Relonchem Oral Solution, identified through a customer complaint.
What consumers should do
s set out in this notification are undertaken for this batch. DMRC reference number DMRC-38460232 Marketing Authorisation Holder Relonchem Limited Medicine Details Gabapentin Relonchem 50mg/ml Oral Solution PL: 20395/0360 Active ingredient: gabapentin SNOMED code: 45344311000001104 GTIN: 5055144203362 Affected Lot Batch Numbers Batch No. Expiry Date Pack Size First Distributed 09E1 01/10/2026 150ML 12/11/2025 11E1 01/10/2026 150ML 12/11/2025 12E1 01/12/2026 150ML 02/01/2026 13E1 01/12/2026 150ML 02/01/2026 14E1 01/12/2026 150ML 20/01/2026 19F1 01/03/2027 150ML 08/04/2026 21F1 01/04/2027 150ML 12/05/2026
Official recall notice
UPDATE: Class 4 Medicines Defect Notification: Relonchem Limited, Gabapentin Relonchem 50mg/ml Oral Solution, EL(26)A/31
Agency: Medicines and Healthcare products Regulatory Agency
Official publication date: June 30, 2026
Read the official UK_MHRA recall notice →SCAN ONCE. KEEP WATCHING.
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