Recall Number: F-0258-2017
Why was Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement. recalled?
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Check out this page for guidance on what to do if you've consumed food from recall F-0258-2017 .
City: Davie
State: Florida
Country: United States
Classification: Class II
Classification Date: 2016-10-25
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Product Description: Cerovite Liquid, 8 oz./236 mL, OTC Non-Sterile. Dietary supplement.
Report Date: 2016-11-02
Product Type: Food
Company: Pharmatech LLC
Status: Terminated
Recall Number: F-0258-2017
Postal Code: 33314-4036
Recall Initiation Date: 2016-08-08
Recall End Date: 2024-09-23
Event ID: 75272
Distribution Pattern: FL, MI, MS, and OH.
Voluntary Or Mandated: Voluntary: Firm initiated
Initial Firm Notification: Letter
Extra Info: UPC No. 005362790590; Lot No. 20471516, 20471517, 20471518, 20471519, & 20471520, Exp. Date 11/2017; Lot No. 20471521, Exp. Date 12/2017; Lot No. 20471601, Exp. Date 01/2018; Lot No. 20471608, Exp. Date 04/2018; Lot No. 20471610 & 20471613, Exp. Date 05/2018; Lot No. 20471614, Exp. Date 06/2018.
Product Quantity: 129,268 bottles
Address: 4131 SW 47th Ave Ste 1403
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