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Class II: temporary or reversible health riskTerminated

L. Perrigo Option 2 Recall

Option 2, Levonorgestrel Tablet, 1

L. Perrigo Company · Allegan, MI

Risk level
Class II
Reported by FDA
Jun 14, 2017
Recall ID
D-0887-2017
Check your lot numberHow we source this data

Summary

L. Perrigo recalled Option 2 starting Jun 1, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0887-2017 on Jun 14, 2017. Reason: Defective Container: Carton is missing the tablet blister strip and tablet. Status: Terminated.

Why it was recalled

Defective Container: Carton is missing the tablet blister strip and tablet.

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

Lot numbers, UPCs & expiration codes

Lot #: 6LV1114, 6LV1115, 6LV1116, 6MV0976, 6MV0977, Exp.04/18; 7AV1173, 7AV1175, 7AV1176, Exp.07/18.

Where it was sold

Nationwide in the US and Canada

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0887-2017
Classification
Class II
Status
Terminated
Recall initiated
Jun 1, 2017
FDA report date
Jun 14, 2017
Quantity
181,776 (units/eaches)
Recall type
Voluntary: Firm initiated
Recalling firm
L. Perrigo Company

Original FDA data

Every field from FDA enforcement report D-0887-2017, exactly as published.

Show all FDA fields
City
Allegan
State
MI
Status
Terminated
Country
United States
Event ID
77397
Address
515 Eastern Ave
Code information
Lot #: 6LV1114, 6LV1115, 6LV1116, 6MV0976, 6MV0977, Exp.04/18; 7AV1173, 7AV1175, 7AV1176, Exp.07/18.
Postal code
49010-9070
Report date
Jun 14, 2017
Product type
Drugs
Recall number
D-0887-2017
Classification
Class II
Recalling firm
L. Perrigo Company
Product quantity
181,776 (units/eaches)
Termination date
Nov 21, 2017
Reason for recall
Defective Container: Carton is missing the tablet blister strip and tablet.
Voluntary / mandated
Voluntary: Firm initiated
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
Distribution pattern
Nationwide in the US and Canada
Recall initiation date
Jun 1, 2017
Initial firm notification
Letter
Center classification date
Jun 6, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0887-2017, published Jun 14, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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