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Class II: temporary or reversible health riskTerminated

Arise & Shine Herbal Products The product is labeled in part "***Arise & Recall

The product is labeled in part "***Arise & Shine Hydrated Bentonite Dietary Supplement…

Arise & Shine Herbal Products, Inc. · Medford, OR

Risk level
Class II
Reported by FDA
Oct 1, 2014
Recall ID
F-2514-2014
Check your lot numberHow we source this data

Summary

Arise & Shine Herbal Products recalled The product is labeled in part "***Arise & starting Jul 23, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2514-2014 on Oct 1, 2014. Reason: Arise & Shine Herbal Products, Inc. is voluntarily recalling Hydrated Bentonite 32 oz liquid pouch due to mis-labeling. The product is labeled as containing 0% Daily Value of iron and actually contains 106% Daily Value of iron. Status: Terminated.

Why it was recalled

Arise & Shine Herbal Products, Inc. is voluntarily recalling Hydrated Bentonite 32 oz liquid pouch due to mis-labeling. The product is labeled as containing 0% Daily Value of iron and actually contains 106% Daily Value of iron.

Product description

The product is labeled in part "***Arise & Shine Hydrated Bentonite Dietary Supplement Extra Thick Formula 32 FL OZ ***% Daily Value Iron 0***Distributed by: Arise & Shine Herbal Products 562 Parsons Drive Medford, Oregon 97501***" Product is packaged in a foil pouch with a plastic screw-on lid. UPC 701088032067

Lot numbers, UPCs & expiration codes

2011 LOT/EXP DATE: 3461106 -12/2014, 3431106 -12/2014, 3411106 -12/2014, 3201106 - 11/2014, 3191106 - 11/2014, 3141106 - 11/2014, 2991106 - 11/2014, 2711106 - 10/2014, 2571106 - 09/2014, 2561106 - 09/2014, 2351106 - 09/2014, 2221106 - 08/2014, 2091106 - 07/2014, 1941106 - 07/2014, 1801106 - 06/2014. 2012 LOT/EXP DATE: 3541206 - 01/2016, 3421206 - 12/2015, 3141206 - 11/2015, 3131206 - 11/2015, 3001206 - 11/2015, 2851206 - 10/2015, 2771206 - 10/2015, 2761206 - 10/2015, 2511206 - 09/2015, 2161206 - 08/2015, 2151206 - 08/2015, 2071206 - 08/2015, 2021206 - 07/2015, 1801206 - 07/2015, 1651206 - 06/2015, 1641206 - 06/2015, 1511206 - 06/2015, 1451206 - 06/2015, 1251206 - 05/2015, 1161206 - 05/2015, 1181206 - 04/2015, 1111206 - 04/2015, 1011206 - 04/2015, 0871206 - 04/2015, 0741206 - 03/2015, 0671206 - 03/2015, 0601206 - 03/2015, 0121206 - 01/2015, 0111206 - 01/2015, 0041206 - 01/2015. 2013 LOT/EXP DATE: 3511306 -12/2016, 3471306 - 12/2016, 3461306 - 12/2016, 3391306 - 12/2016, 3381306 - 12/2016, 3111306 - 11/2016, 3041306 - 11/2016, 2911306 - 10/2016, 2901306 - 10/2016, 2831306 - 10/2016, 2771306 - 10/2016, 2621306 - 09/2016, 2611306 - 09/2016, 2331306 - 08/2016, 2321306 - 08/2016, 2201306 - 08/2016, 2191306 - 08/2016, 1991306 - 07/2016, 1981306 - 07/2016, 1651306 - 06/2016, 1641306 - 06/2016, 1361306 - 06/2016, 1351306 - 06/2016, 1281306 - 05/2016, 1271306 - 05/2016, 1231306 - 05/2016, 1221306 - 05/2016, 0931306 - 04/2016, 0921306 - 04/2016, 0731306 - 03/2016, 0721306 - 03/2016, 0651306 - 03/2016, 0531306 - 03/2016, 0391306 - 02/2016, 0311306 - 02/2016, 0171306 - 01/2016, 0151306 - 01/2016, 0091306 - 01/2016. 2014 LOT/EXP DATE: 1551406 - 06/2017,1501406 - 06/2017,1291406 - 05/2017,1271406 - 05/2017,1121406 - 04/2017,1071406 - 04/2017,0711406 - 03/2017,0781406 - 03/2017,0771406 - 03/2017,0571406 - 03/2017,0561406 - 03/2017,0431406 - 02/2017,0421406 - 02/2017,0221406 - 01/2017,0211406 - 01/2017. Code breakdown: Lot # 0091306: 009 (Julian date) 13 (year of 2013) 06 (Product identifier) 01/2016 (Expiration date)

Where it was sold

Product is distributed worldwide.

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-2514-2014
Classification
Class II
Status
Terminated
Recall initiated
Jul 23, 2014
FDA report date
Oct 1, 2014
Quantity
Approximately 24,794 / 32 oz pouches.
Recall type
Voluntary: Firm initiated
Recalling firm
Arise & Shine Herbal Products, Inc.

Original FDA data

Every field from FDA enforcement report F-2514-2014, exactly as published.

Show all FDA fields
City
Medford
State
OR
Status
Terminated
Country
United States
Event ID
68903
Address
562 Parsons Dr Ste 116
Code information
2011 LOT/EXP DATE: 3461106 -12/2014, 3431106 -12/2014, 3411106 -12/2014, 3201106 - 11/2014, 3191106 - 11/2014, 3141106 - 11/2014, 2991106 - 11/2014, 2711106 - 10/2014, 2571106 - 09/2014, 2561106 - 09/2014, 2351106 - 09/2014, 2221106 - 08/2014, 2091106 - 07/2014, 1941106 - 07/2014, 1801106 - 06/2014. 2012 LOT/EXP DATE: 3541206 - 01/2016, 3421206 - 12/2015, 3141206 - 11/2015, 3131206 - 11/2015, 3001206 - 11/2015, 2851206 - 10/2015, 2771206 - 10/2015, 2761206 - 10/2015, 2511206 - 09/2015, 2161206 - 08/2015, 2151206 - 08/2015, 2071206 - 08/2015, 2021206 - 07/2015, 1801206 - 07/2015, 1651206 - 06/2015, 1641206 - 06/2015, 1511206 - 06/2015, 1451206 - 06/2015, 1251206 - 05/2015, 1161206 - 05/2015, 1181206 - 04/2015, 1111206 - 04/2015, 1011206 - 04/2015, 0871206 - 04/2015, 0741206 - 03/2015, 0671206 - 03/2015, 0601206 - 03/2015, 0121206 - 01/2015, 0111206 - 01/2015, 0041206 - 01/2015. 2013 LOT/EXP DATE: 3511306 -12/2016, 3471306 - 12/2016, 3461306 - 12/2016, 3391306 - 12/2016, 3381306 - 12/2016, 3111306 - 11/2016, 3041306 - 11/2016, 2911306 - 10/2016, 2901306 - 10/2016, 2831306 - 10/2016, 2771306 - 10/2016, 2621306 - 09/2016, 2611306 - 09/2016, 2331306 - 08/2016, 2321306 - 08/2016, 2201306 - 08/2016, 2191306 - 08/2016, 1991306 - 07/2016, 1981306 - 07/2016, 1651306 - 06/2016, 1641306 - 06/2016, 1361306 - 06/2016, 1351306 - 06/2016, 1281306 - 05/2016, 1271306 - 05/2016, 1231306 - 05/2016, 1221306 - 05/2016, 0931306 - 04/2016, 0921306 - 04/2016, 0731306 - 03/2016, 0721306 - 03/2016, 0651306 - 03/2016, 0531306 - 03/2016, 0391306 - 02/2016, 0311306 - 02/2016, 0171306 - 01/2016, 0151306 - 01/2016, 0091306 - 01/2016. 2014 LOT/EXP DATE: 1551406 - 06/2017,1501406 - 06/2017,1291406 - 05/2017,1271406 - 05/2017,1121406 - 04/2017,1071406 - 04/2017,0711406 - 03/2017,0781406 - 03/2017,0771406 - 03/2017,0571406 - 03/2017,0561406 - 03/2017,0431406 - 02/2017,0421406 - 02/2017,0221406 - 01/2017,0211406 - 01/2017. Code breakdown: Lot # 0091306: 009 (Julian date) 13 (year of 2013) 06 (Product identifier) 01/2016 (Expiration date)
Postal code
97501-3793
Report date
Oct 1, 2014
Product type
Food
Recall number
F-2514-2014
Classification
Class II
Recalling firm
Arise & Shine Herbal Products, Inc.
Product quantity
Approximately 24,794 / 32 oz pouches.
Termination date
Nov 19, 2014
Reason for recall
Arise & Shine Herbal Products, Inc. is voluntarily recalling Hydrated Bentonite 32 oz liquid pouch due to mis-labeling. The product is labeled as containing 0% Daily Value of iron and actually contains 106% Daily Value of iron.
Voluntary / mandated
Voluntary: Firm initiated
Product description
The product is labeled in part "***Arise & Shine Hydrated Bentonite Dietary Supplement Extra Thick Formula 32 FL OZ ***% Daily Value Iron 0***Distributed by: Arise & Shine Herbal Products 562 Parsons Drive Medford, Oregon 97501***" Product is packaged in a foil pouch with a plastic screw-on lid. UPC 701088032067
Distribution pattern
Product is distributed worldwide.
Recall initiation date
Jul 23, 2014
Initial firm notification
E-Mail
Center classification date
Sep 22, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2514-2014, published Oct 1, 2014. View the source record (openFDA) · FDA enforcement reports

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

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