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Class II: temporary or reversible health riskTerminated

Perrigo of SC EstroPlus Maximum Strength Menopause Support Recall

EstroPlus Maximum Strength Menopause Support Dietary Supplement in 28 count and 56 coun…

Perrigo of SC · Greenville, SC

Risk level
Class II
Reported by FDA
Jan 15, 2014
Recall ID
F-1384-2014
Check your lot numberHow we source this data

Summary

Perrigo of SC recalled EstroPlus Maximum Strength Menopause Support starting Nov 25, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1384-2014 on Jan 15, 2014. Reason: Potential presence of Chloramphenicol contamination. Status: Terminated.

Why it was recalled

Potential presence of Chloramphenicol contamination

Product description

EstroPlus Maximum Strength Menopause Support Dietary Supplement in 28 count and 56 count blister strips under the following labels - CareOne Maximum Strength Multi Symptom Menopause Formula, 28 Caplets/Dietary Supplement; Meijer Maximum Strength Estroplus, Dietary Supplement, 28 Caplets; TopCare Maximum Strength Estroplus Dietary Supplement, 28 Caplets; Sunmark Estroplus Extra Strength, Dietary Supplement, 56 Caplets; Health Mart Pharmacy Extra Strength Estroplus, 56 Caplets Dietary Supplement; Up&Up Estroplus Dietary Supplement Maximum Strength 28 Caplets; CareOne Extra Strength Estroplus 56 Caplets/Dietary Supplement; Western Family Extra Strength Estroplus 56 Caplets, Meijer Extra Strength Estroplus Dietary Supplement 56 Caplets; Publix Extra Strength Estroplus 56 Caplets, Dietary Supplement; and TopCare Extra Strength Estroplus Dietary Supplement 56 Caplets.

Lot numbers, UPCs & expiration codes

3FN0981 (Exp 04/15), 3FN1338 (Exp 04/15), 3FN1116 (Exp 04/15), 3EN1050 (Exp 04/15), 3JN1230 (Exp 04/15), 3KN1691 (Exp 05/15), 3KN1207 (Exp. 05/15), 3JN1013 (05/15), 3JN1077 (Exp 05/15), 3HN1293 (Exp 05/15), 1KN1496 (Exp 05/14), 1JN1234 (Exp 05/14), 1KN1775 (Exp. 05/14), 1LN1254 (Exp 05/14), 1LN1867 (Exp 05/14), 1MN1647 (Exp 05/14), 2AN1562 (Exp 10/14), 2AN1595 (Exp 10/14), 2BN2120 (Exp 01/15), 2DN1514 (Exp 01/15), 2DN1515 (Exp 10/14), 2DN1608 (Exp 05/14), 2DN1997 (Exp 01/15), 2EN2099 (Exp. 01/15), 2FN1524 (Exp 03/15), 2FN1923 (Exp 03/15), 2FN1939 (Exp 01/15), 2GN1806 (Exp 03/15), 2HN1412 (Exp 03/15), 2HN1496 (Exp 03/15), 2JN1383 (Exp 03/15), 2MN1156 (Exp 03/15), 3AN1835 (Exp 03/15), 3BN1683 (Exp 03/15), 3DN1482 (Exp 03/15), 3FN1132 (Exp 03/15)

Where it was sold

FL, IL, MI, MN, OR, PA & TX

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1384-2014
Classification
Class II
Status
Terminated
Recall initiated
Nov 25, 2013
FDA report date
Jan 15, 2014
Quantity
68,534 (units/eaches)
Recall type
Voluntary: Firm initiated
Recalling firm
Perrigo of SC

Original FDA data

Every field from FDA enforcement report F-1384-2014, exactly as published.

Show all FDA fields
City
Greenville
State
SC
Status
Terminated
Country
United States
Event ID
66943
Address
4615 Dairy Dr
Code information
3FN0981 (Exp 04/15), 3FN1338 (Exp 04/15), 3FN1116 (Exp 04/15), 3EN1050 (Exp 04/15), 3JN1230 (Exp 04/15), 3KN1691 (Exp 05/15), 3KN1207 (Exp. 05/15), 3JN1013 (05/15), 3JN1077 (Exp 05/15), 3HN1293 (Exp 05/15), 1KN1496 (Exp 05/14), 1JN1234 (Exp 05/14), 1KN1775 (Exp. 05/14), 1LN1254 (Exp 05/14), 1LN1867 (Exp 05/14), 1MN1647 (Exp 05/14), 2AN1562 (Exp 10/14), 2AN1595 (Exp 10/14), 2BN2120 (Exp 01/15), 2DN1514 (Exp 01/15), 2DN1515 (Exp 10/14), 2DN1608 (Exp 05/14), 2DN1997 (Exp 01/15), 2EN2099 (Exp. 01/15), 2FN1524 (Exp 03/15), 2FN1923 (Exp 03/15), 2FN1939 (Exp 01/15), 2GN1806 (Exp 03/15), 2HN1412 (Exp 03/15), 2HN1496 (Exp 03/15), 2JN1383 (Exp 03/15), 2MN1156 (Exp 03/15), 3AN1835 (Exp 03/15), 3BN1683 (Exp 03/15), 3DN1482 (Exp 03/15), 3FN1132 (Exp 03/15)
Postal code
29607-3792
Report date
Jan 15, 2014
Product type
Food
Recall number
F-1384-2014
Classification
Class II
Recalling firm
Perrigo of SC
Product quantity
68,534 (units/eaches)
Termination date
Nov 10, 2014
Reason for recall
Potential presence of Chloramphenicol contamination
Voluntary / mandated
Voluntary: Firm initiated
Product description
EstroPlus Maximum Strength Menopause Support Dietary Supplement in 28 count and 56 count blister strips under the following labels - CareOne Maximum Strength Multi Symptom Menopause Formula, 28 Caplets/Dietary Supplement; Meijer Maximum Strength Estroplus, Dietary Supplement, 28 Caplets; TopCare Maximum Strength Estroplus Dietary Supplement, 28 Caplets; Sunmark Estroplus Extra Strength, Dietary Supplement, 56 Caplets; Health Mart Pharmacy Extra Strength Estroplus, 56 Caplets Dietary Supplement; Up&Up Estroplus Dietary Supplement Maximum Strength 28 Caplets; CareOne Extra Strength Estroplus 56 Caplets/Dietary Supplement; Western Family Extra Strength Estroplus 56 Caplets, Meijer Extra Strength Estroplus Dietary Supplement 56 Caplets; Publix Extra Strength Estroplus 56 Caplets, Dietary Supplement; and TopCare Extra Strength Estroplus Dietary Supplement 56 Caplets.
Distribution pattern
FL, IL, MI, MN, OR, PA & TX
Recall initiation date
Nov 25, 2013
Initial firm notification
Letter
Center classification date
Jan 8, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1384-2014, published Jan 15, 2014. View the source record (openFDA) · FDA enforcement reports

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

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