American Health Packaging on behalf of BluePoint Laboratories is voluntarily recalling 21
batches of Potassium Chloride Extended-Release Capsules, USP (750mg) 10 mEq K, to the consumer level. The product is being recalled because of failed dissolution.
Potassium Chloride Extended-Release Capsules are used for the treatment of patients with low potassium (hypokalemia) and are packaged in bottles of 100-count (NDC 68001-396-00) and 500-count (NDC 68001-396-03) capsules
Consumers that have Potassium Chloride Extended-Release Capsules subject to the recall should consult
with their physician or health care provider before they stop using the product. Consumers should also
contact their physician or healthcare provider if they have experienced any problems that may be related
to taking or using this drug product. Consumers should call Sedgwick, a recall solution vendor, at 1-855-
695-8564, Monday – Friday, 8:00 am – 5:00 pm EST for return instructions and further information. (Note: One Benecard Central Fill member was affected by this recall and member outreach was completed.)\
