Smyrna, TN, Vi-Jon, LLC expands recall of lemon flavor constipation products
The recall follows testing that identified the presence of Gluconacetobacter liquefaciens. It could put immunocomprised patients at risk for invasive infections.
News 12 Staff
•
Jul 18, 2022, 8:51 AM
•
Updated 638 days ago
Share:
More Stories
3:49
be Well: Best beauty products that are also great for the environment
6h ago0:18
2 best friends from New Jersey split $1 million Powerball prize
yesterday0:28
New Jersey Turnpike Authority warns users of text message scam
yesterday1:47
Food labels can sometimes be misleading. Kane In Your Corner explains what to look out for.
yesterday0:51
IRS warns public about potential tax scams as Tax Day deadline approaches
3ds ago1:37
The Real Deal: How to save the next time you dine out
4ds ago3:49
be Well: Best beauty products that are also great for the environment
6h ago0:18
2 best friends from New Jersey split $1 million Powerball prize
yesterday0:28
New Jersey Turnpike Authority warns users of text message scam
yesterday1:47
Food labels can sometimes be misleading. Kane In Your Corner explains what to look out for.
yesterday0:51
IRS warns public about potential tax scams as Tax Day deadline approaches
3ds ago1:37
The Real Deal: How to save the next time you dine out
4ds agoSmyrna, TN, Vi-Jon, LLC is expanding its recall of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor (10-fluid-ounce).
The product is used for relief of constipation and was distributed nationwide to wholesale and retail outlets.
The recall follows testing that identified the presence of Gluconacetobacter liquefaciens. It could put immunocomprised patients at risk for invasive infections.
These are the affected brands:
The company says it has so far received one report of an adverse reaction.
The company advises anyone who has these product to stop using them and return it to the place of purchase. Questions can be directed to Vi-Jon, LLC by e-mail (Recalls@Vijon.com) Monday-Friday, from 7:30 a.m. to 4:30 p.m., Central Time. Anyone experiencing issues from taking the product should contact their physician or health care provider and report the issue to the Food and Drug Administration's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Complete and submit the report Online
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
