The Recall Desk
ModerateFDA (Drugs)·D-1196-2018·Announced 2018-09-26

Beaumont Bio-Med Recalls Muscle & Joint Pain Relief Spray for CGMP Deviations

Beaumont Bio-Med, Inc. is recalling 109 bottles of Muscle & Joint Pain Relief Homeopathic Formula due to CGMP deviations that could result in possible microbial contamination.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II and involves a theoretical risk of microbial contamination without reported illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Beaumont Bio-Med, Inc. is recalling 109 bottles of Muscle & Joint Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle. The product is identified by NDC 58066-7041-7, Lot 012916F, and an expiration date of 01/2019.

The recall was initiated due to Current Good Manufacturing Practice (CGMP) deviations. The products were manufactured by a contract manufacturer under conditions that could result in possible microbial contamination.

The affected product was distributed nationwide in the USA. Consumers should stop using the product and contact the recalling firm for further instructions.

The recalled product

Product
Muscle & Joint Pain Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7041-7
Affected units
109

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot: 012916F
  • Exp 01/2019

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 8 recalled by Beaumont Bio-med, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 8 products in this recall →