Acyclovir Tablets, USP, 400 mg, 50 Tablets (5 x 10) unit dose blisters [NDC 50268-061-11] per carton [NDC 50268-061-15], Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478
Reported: March 7, 2018 Initiated: February 9, 2018 #D-0544-2018
Product Description
Acyclovir Tablets, USP, 400 mg, 50 Tablets (5 x 10) unit dose blisters [NDC 50268-061-11] per carton [NDC 50268-061-15], Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478
Reason for Recall
Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.
Details
- Recalling Firm
- Apace KY LLC
- Units Affected
- 630 cartons
- Distribution
- Nationwide
- Location
- Fountain Run, KY
Frequently Asked Questions
What product was recalled? ▼
Acyclovir Tablets, USP, 400 mg, 50 Tablets (5 x 10) unit dose blisters [NDC 50268-061-11] per carton [NDC 50268-061-15], Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478. Recalled by Apace KY LLC. Units affected: 630 cartons.
Why was this product recalled? ▼
Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 7, 2018. Severity: Moderate. Recall number: D-0544-2018.
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