D-0887-2017 Class II Terminated
FDA drug recall D-0887-2017 was initiated by L. Perrigo Company on Jun 1, 2017 and is designated Class II. Reason for recall: Defective Container: Carton is missing the tablet blister strip and tablet. The recall status is terminated (terminated Nov 21, 2017). Affected quantity: 181,776 (units/eaches).
Recall Details
- Product Type
- Drugs
- Report Date
- Jun 14, 2017
- Initiation Date
- Jun 1, 2017
- Termination Date
- Nov 21, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 181,776 (units/eaches)
Product Description
Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI 49010. NDC 0113-2003-12
Reason for Recall
Defective Container: Carton is missing the tablet blister strip and tablet.
Distribution Pattern
Nationwide in the US and Canada
Code Information
Lot #: 6LV1114, 6LV1115, 6LV1116, 6MV0976, 6MV0977, Exp.04/18; 7AV1173, 7AV1175, 7AV1176, Exp.07/18.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0887-2017
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026