Class 2 medicines recall: Medikinet XL 20mg modified-release capsules (methylphenidate hydrochloride)
Read the official alert on GOV.UK — MedRegWatch re-presents it; GOV.UK is the authoritative source.
| Class | Class 2 |
|---|---|
| Type | Medicines recall/notification |
| Issued | 14 Jun 2016 |
| Reference | EL (16)A/08 |
Product information
EL number
EL (16)A/08
MDR number
MDR 047-06/16
Company name
B&S Healthcare
Product description
| Batch Number | Expiry Date | Pack Size | First distributed |
|---|---|---|---|
| 02L3602 | 01/2018 | 30 capsules | 07/04/2016 |
| 02L3603 | 06/2018 | 30 capsules | 06/04/2016 |
Brief description of the problem
B&S Healthcare are recalling two batches of parallel imported Medikinet XL 20mg modified-release capsules that have been incorrectly repackaged in 30mg cartons.
The 20 mg strength is correctly stated on the blister packs. See Appendix 1 of the document below for photograph of a sample pack.
Pharmacists and wholesalers are asked to return any remaining stock from these batches to B & S Healthcare.
For medical information, please contact telephone number 0208 515 3735.
For enquiries regarding returns please contact telephone number 0208 728 7800.
Download document
Medikinet XL 20mg modified-release capsules - class 2 recall
Recipients of this Drug Alert should bring it to the attention of relevant contacts by copy of this letter. Local area teams are asked to forward this to relevant clinics, general practitioners and community pharmacists for information.