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Class II: temporary or reversible health riskTerminated

Wynlife Healthcare All-In-One Probiotics Recall

All-In-One Probiotics, K12-BB12-LB3

Wynlife Healthcare, Inc. · San Diego, CA

Risk level
Class II
Reported by FDA
Mar 27, 2013
Recall ID
F-1244-2013
Check your lot numberHow we source this data

Summary

Wynlife Healthcare recalled All-In-One Probiotics starting May 31, 2011. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1244-2013 on Mar 27, 2013. Reason: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents. Status: Terminated.

Why it was recalled

Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.

Product description

All-In-One Probiotics, K12-BB12-LB3; Dietary Supplement; 30 Packets;Serving size 2 Tablets (1 Packet)l L141/1. Adults take 2 to 4 tablets daily; Children: take 1 to 2 tablets daily (or as directed by your healthcare practitioner. Chew slowly or allow to dissolve in mouth. Manufactured for Wynlife Healthcare, Inc., San Diego, CA 92130.

Lot numbers, UPCs & expiration codes

PN 141; Lot #'s: 100521 and 110099

Where it was sold

Nationwide distribution.

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-1244-2013
Classification
Class II
Status
Terminated
Recall initiated
May 31, 2011
FDA report date
Mar 27, 2013
Quantity
456 boxes
Recall type
Voluntary: Firm initiated
Recalling firm
Wynlife Healthcare, Inc.

Original FDA data

Every field from FDA enforcement report F-1244-2013, exactly as published.

Show all FDA fields
City
San Diego
State
CA
Status
Terminated
Country
United States
Event ID
64513
Address
12707 High Bluff Dr Ste 200
Code information
PN 141; Lot #'s: 100521 and 110099
Postal code
92130-2037
Report date
Mar 27, 2013
Product type
Food
Recall number
F-1244-2013
Classification
Class II
Recalling firm
Wynlife Healthcare, Inc.
Product quantity
456 boxes
Termination date
Mar 21, 2013
Reason for recall
Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.
Voluntary / mandated
Voluntary: Firm initiated
Product description
All-In-One Probiotics, K12-BB12-LB3; Dietary Supplement; 30 Packets;Serving size 2 Tablets (1 Packet)l L141/1. Adults take 2 to 4 tablets daily; Children: take 1 to 2 tablets daily (or as directed by your healthcare practitioner. Chew slowly or allow to dissolve in mouth. Manufactured for Wynlife Healthcare, Inc., San Diego, CA 92130.
Distribution pattern
Nationwide distribution.
Recall initiation date
May 31, 2011
Initial firm notification
Letter
Center classification date
Mar 21, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1244-2013, published Mar 27, 2013. View the source record (openFDA) · FDA enforcement reports

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

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