Lidocaine Patch 5%, 30-count carton, Rx only, MFG: Qualitest Products, NDC 0603-1880-16
Check against the official notice below — it lists the full affected range.
McKesson Medical-Surgical Inc. is recalling Lidocaine Patch 5% in 30-count cartons manufactured by Qualitest Products due to temperature abuse during storage or handling that violated good manufacturing practice standards. The recalled product was distributed nationwide, with a total of 3 cartons containing 30 pouches each affected by this issue. Because McKesson cannot identify which specific lot numbers were received by individual customers, the company has provided distribution dates to help customers determine if their product may be impacted.
The source document does not specify what action affected consumers should take regarding this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
cGMP deviations: Temperature abuse
Reason for recall: cGMP deviations: Temperature abuse Distribution: USA nationwide. Quantity: 3 cartons/30 pouches per carton Lot/code info: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Official record: FDA (Drug enforcement) ↗
Republished from the official source above; details can change — the source record controls.