OsteoSheath 4 (Vinco) – Salmonella contamination (2013)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vinco's OsteoSheath 4 Enhanced Bone Support, Calcium Supplement, 120 Tablets, distributed by Vinco, Inc., Evans City, PA
Brand
Vinco Inc.
Lot Codes / Batch Numbers
Osteosheath 4 UPC 739930275195, lot numbers 11060198 through 1106199, 11100897through 1110898, 1204780 through 1204781, 120101089 through 120101090, 13020640 through 13020641 with expiration dates 10/13 to 2/15.
Products Sold
Osteosheath 4 UPC 739930275195, lot numbers 11060198 through 1106199, 11100897through 1110898, 1204780 through 1204781, 120101089 through 120101090, 13020640 through 13020641 with expiration dates 10/13 to 2/15.
Vinco Inc. is recalling Vinco's OsteoSheath 4 Enhanced Bone Support, Calcium Supplement, 120 Tablets, distributed by Vinco, due to The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4 was potentially contaminated with Salmonella.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4 was potentially contaminated with Salmonella.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026