The Recall Desk
HighFDA (Drugs)·D-0717-2018·Announced 2018-05-02

Coastal Meds Recalls Cyanocobalamin Injectable Due to Particulate Matter

Coastal Meds, LLC. is recalling 745 vials of Cyanocobalamin Injectable due to the presence of unknown particulate matter.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II and involves a risk-of-harm product (injection) where injury has not yet been reported, fitting the 'High' severity criteria.

Plain-English summary

Coastal Meds, LLC. is recalling 745 vials of CYANOCOBALAMIN Injectable-30 mL MDV. The recall was initiated because of the presence of unknown particulate matter in the product.

The affected product was distributed nationwide in the USA. The specific lots involved are C/010218 (Discard by 07/01/2018), CAC/013118 (Discard by 4/1/2018), CAC/020518 (Discard by 4/6/2018), and CAC/021418 (Discard by 4/15/2018).

Consumers and healthcare providers should stop using the recalled product and contact Coastal Meds, LLC. for further instructions or a refund.

The recalled product

Product
CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
Manufacturer
Coastal Meds, LLC.
Affected units
745

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 (4)

  • Lot: C/010218 Discard by 07/01/2018
  • CAC/013118 Discard by 4/1/2018
  • CAC/020518 Discard by 4/6/2018
  • CAC/021418 Discard by 4/15/2018

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 10 recalled by Coastal Meds, LLC. 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 10 products in this recall →