Recalls & Alerts Published by NAFDAC

Tuesday, 22 November 2016 07:45

Recall Of Respontin Nebules In Dublin

The National Agency for Food and Drug Administration and Control has been informed that the Irish Health Product Regulatory Authority, Dublin announced the recall of four (4) batches of Respontin Nebules 250 microgram/1ml Respontin Nebules five hundred (500) microgram/2ml (Ipratropium Bromide) by GlaxoSmithKline over out of specification results for impurities .

Respontin Nebules is indicated for the treatment of reversible airway obstruction. It is used in a nebulizer, a machine that converts the liquid medicine inside the nebules into particles that can be inhaled.

The details of the recalled product are as follows:

i.   Batch Number: B76315Ba

Expiry date: 28/02/2017

Pack Size: 20x1ml

First distributed: 30th March, 2015

ii.   Batch Number: B85515J

Expiry date: 31/10/2017

Pack Size: 20x1ml

First distributed: 27th January, 2015

iii.  Batch Number: B76315BA

Expiry date: 28/02/2017

Pack Size: 4x5x2ml

First distributed: 29th May, 2015

iv.  Batch Number: B85515J

Expiry date: 31/10/2017

Pack Size: 4x5x2ml

First distributed: 18th December, 2015

Healthcare providers with stock of the products should immediately discontinue the administration or use of the products.

Healthcare professionals and consumers should report adverse events to NAFDAC PRASCOR (20543-Toll free from all networks) or via This email address is being protected from spambots. You need JavaScript enabled to view it.

 

NAFDAC…..Safeguarding the health of the Nation!!!

The National Agency for Food and Drug Administration and Control hereby informs the general public of the recall of some drugs manufactured by Ta Fong Pharmaceutical Company Limited, over quality concerns.

The affected products are;

  1. Urodine F.C. Tablets SGP-56569
  2. Dicokan Tablets (30mg) SGP-56102
  3. Toeefon Tablets (250mg) SGP-56387
  4. Shoren Suppositories (12mg) SGP-60943
  5. Molin Tablets (10mg) SGP-62483
  6. Famoster Film coated Tablets (20mg) SGP-62850
  7. Lincomycin solution for injection (300mg/ml) HK-61712
  8. Clindamycin Capsules (150mg) SGP-64191

The products are not registered by NAFDAC.

The importers and the general public are implored to avoid the importation, purchase or use of these products.

Any information on the distribution and sale of the product should be reported to the nearest NAFDAC office, NAFDAC PRASCOR (20543- TOLL FREE from all networks) or via This email address is being protected from spambots. You need JavaScript enabled to view it.

 

NAFDAC…Safeguarding the health of the Nation!!!

Thursday, 19 May 2016 00:00

Recall Of Spotchem II Test Strips

The National Agency for Food and Drug Administration and Control hereby inform all healthcare professionals of the recall of Spotchem II Basic Panel-1 Reagent Test Strip and Spotchem II Glucose Reagent Test Strips by Singaporean Health Authorities. The products which are used in testing blood sugar level were recalled over inaccurate blood sugar reading, which may result in fatalities. The products are said to be distributed worldwide between 18th February, 2015 and 13th October, 2015.

Details of the affected lots are as follows:

Product Manufacturer: Arkay Pharmaceuticals, India

Manufacturing Dates:   Between November, 2014 and September, 2015

Lot Numbers:                 PN5C26 and EA4M78

Quantity Affected:         99 boxes (25 foiled packaged test strips per box)

NAFDAC implores importers and healthcare providers to discontinue the purchase, administration or use of these products.

NAFDAC implores all outlets with stock of this product to immediately remove them from circulation. 

Healthcare professionals and consumers should report adverse events to NAFDAC PRASCOR (20543-Toll free from all networks) or via This email address is being protected from spambots. You need JavaScript enabled to view it.

NAFDAC…..Safeguarding the health of the Nation!!!

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