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An official FDA notice concerns Apotex - safety alert. An official FDA notice concerns Apotex. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-06-13. Lots: NJ4501. Recall numbers: D-0841-2018. Check the official notice for the complete list. Published 2018-06-13.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Recall number
D-0841-2018
Official notice
2018-06-13
The hazard
The hazard
An official FDA notice concerns Apotex. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-06-13. Lots: NJ4501. Recall numbers: D-0841-2018. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Lots
Event Ids
Recall Numbers
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Turn on recall alertsWhere it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Affected area 2
Company & contacts
Company & contacts
Brand: Apotex. Contact: Apotex Inc..
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
a product listed in the official notice - safety alert
Apo-fluoxetine: the impurities are out of specification and out of trend
Extra strength ibuprofen liquid gel capsules: presence of cloudy capsules in affected lots
Apo-brimonidine-timop: the weight is out of specification in the affected lot.
Apo-candesartan: affected lots were manufactured using an active ingredient that was out of specification for dissolution
Apo-travoprost-timop pq: missing the documented justification for the results obtained.
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