CLASS II Food recall · Reported 27 Mar 2013 · FDA Enforcement Report
All-In-One Probiotics, K12-BB12-LB3 recalled by Wynlife Healthcare
Wynlife Healthcare is recalling All-In-One Probiotics, K12-BB12-LB3, 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-1244-2013
- FDA event ID
- 64513
- Recalling firm
- Wynlife Healthcare, San Diego, CA
- 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
- Probiotics
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
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.
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 141; Lot #'s: 100521 and 110099
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 64513This product is part of a recall event; the main page for the event is Vegi-Fiber Plus recalled by Wynlife Healthcare.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Vegi-Fiber Plus recalled by Wynlife HealthcareVegi-Fiber Plus | Wynlife Healthcare | Other | Nationwide |
More recalls from Wynlife Healthcare
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Vegi-Fiber Plus recalled by Wynlife HealthcareVegi-Fiber Plus | Wynlife Healthcare | Other | Nationwide |
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|---|---|---|---|---|---|
| Food | CLASS II | Neuro Nourish dietary supplement;-1 Prebiotic, Probiotic recalledNeuro Nourish | Sensory Supplement | Other | Nationwide |
| Food | CLASS I | SunBiotics Activated Almonds Infused with Probiotics recalledSunBiotics Activated | Windy City Organics | Salmonella | 7 states |
| Food | CLASS II | Biostime Kids Calm & Sleep Support Fruity Bites Probiotics recalledBiostime Kids | Health and Happiness (H&H) | Foreign Material | CA, IL, TN |
| Food | CLASS II | ZOE Daily 30+ Prebiotic blend recalled by Zoe USZoe | Zoe US | Foreign Material | 26 states |
| Food | CLASS I | Mt. Capra Goat Milk Formula Recipe Kit recalled by Healthwest MineralsMt. Capra | Healthwest Minerals | Packaging Defects | Nationwide |