CLASS II Food recall · Reported 27 Mar 2013 · FDA Enforcement Report
Vegi-Fiber Plus recalled by Wynlife Healthcare
Wynlife Healthcare is recalling Vegi-Fiber Plus, distributed nationwide in the US. The recall was initiated on 31 May 2011 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1243-2013
- FDA event ID
- 64513
- Recalling firm
- Wynlife Healthcare, San Diego, CA
- Brand
- Vegi-Fiber Plus
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 31 May 2011
- FDA classified
- 21 Mar 2013
- Reported
- 27 Mar 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 31 May 2011 | Recall initiated by company | |
| 21 Mar 2013 | Classified by FDA | +660 days |
| 27 Mar 2013 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.
Product as listed by the FDA
Vegi-Fiber Plus; O Trans Fat; only 15.4 Calories; Dietary Supplement; 60 Packets; Scientific formula for Natural Vitality; 15 Vegetable and Fruit Extracts; Newest Japanese Carbohydrate Blocker: Fibersol -2; Each Packet Contains 3.5g of Water-Soluble Dietary Fiber. Manufactured for Wynlife Healthcare, Inc., San Diego, CA 92130.
Where it was distributed
Nationwide distribution.
Questions about this recall
Why was it recalled?
Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber Plus products due to DEHP contaminated clouding agents.
Which lots are affected?
PN 135; Lot #'s: 090336 and 100340
Where was it sold?
Nationwide distribution.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 64513| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | All-In-One Probiotics, K12-BB12-LB3 recalled by Wynlife HealthcareAll-In-One Probiotics | Wynlife Healthcare | Other | Nationwide |
More recalls from Wynlife Healthcare
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | All-In-One Probiotics, K12-BB12-LB3 recalled by Wynlife HealthcareAll-In-One Probiotics | Wynlife Healthcare | Other | Nationwide |
Other Dietary Supplements recalls
All 733| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |