Home / Pets Training / RECALL ALERT: Phenobarbital Pet Seizure Medication Recalled Due to Serious Labeling Error

RECALL ALERT: Phenobarbital Pet Seizure Medication Recalled Due to Serious Labeling Error

Certain bottles of the anti-convulsant, anti-seizure medicine, Phenobarbital, manufactured by means of C.O. Truxton, Inc., are being recalled after bottles containing 30mg capsules had been mislabeled as 15mg, posing a major possibility of overdose to cats and canines taking the prescribed medicine.

This mislabeled product may reveal the patron or their puppy(s) to doable overdosing that may purpose critical intoxication which would possibly lead to cardiogenic surprise, renal failure, coma or loss of life.

phenobarbital

Bellmawr, New Jersey, C.O. Truxton, Inc. is voluntarily recalling lot 70952A of Phenobarbital Tablets, USP, 15 mg, to the patron/consumer degree. The producer won a showed buyer grievance bottle categorized as phenobarbital 15 mg was once discovered to include phenobarbital 30 mg capsules.

C.O. Truxton, Inc. has now not won any studies of inauspicious occasions comparable to this recall.

The product is indicated to be used as a sedative or anticonvulsant and is packaged in 1000 depend bottles, NDC 0463-6160-10, UPC 7 0463616010 6, lot quantity 70952A, expiration date 11/17.

The 15 mg Tablet is debossed with “West-ward 445” on one aspect and clean at the opposite aspect; the 30 mg Tablet is debossed with “West-ward 450” on one aspect and scored at the opposite aspect. The product was once dispensed Nationwide in america to Physician & Veterinarian Treatment Centers.

C.O. Truxton, Inc. is notifying all shoppers on report who bought the affected product by way of US Mail which incorporates a recall letter, recall reaction shape and is arranging for complete credit score returns, replacements, and many others. of all recalled product. Consumers/vendors/shops that experience recalled product must prevent the usage of the product and go back their product to their position of acquire.

Consumers with questions referring to this recall can touch C.O Truxton, Inc. by means of telephone at (856) 933-2333, Monday to Friday between 9am and 5pm (EST).  Consumers must touch their doctor or healthcare supplier if they have got skilled any issues that can be comparable to taking or the usage of this drug product.

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