Every recall we track for H J Harkins Company Inc dba Pharma Pac — 9 in all, from 2018–2020 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls on record by year — 9 drug.
Pharma Pac recalls acetaminophen-codeine tablets due to cGMP deviations. Products sold in 10-60 count bottles with specific NDC numbers. No remedy provided in official notice.
Pharma Pac recalls 30-count, 42-count, 45-count, and 50-count acetaminophen 500mg tablets due to foreign tablets being commingled in some bottles. Consumers should check their bottles for foreign tablets and contact the company for guidance.
Pharma Pac recalls 150mg Ranitidine tablets with NDMA impurity detected. Affected lots expire May 2024 through November 2024. Stop using immediately.
Pharma Pac recalls Neomycin 3.5 mg/g ophthalmic ointment due to insufficient quality assurance controls in manufacturing. This product was sold with specific lot numbers and expiration dates.
Pharma Pac recalls acetaminophen children's liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii bacteria. Affected lots manufactured in Levittown, PA. Consumers should contact the company for details.
Pharma Pac recalls Losartan Potassium 100mg tablets due to traces of NMBA impurity found in the active ingredient. Affected products have specific NDC and lot numbers. Consumers should contact the company for details.
Pharma Pac recalls GENTAMICIN OPTH-SOL 5ml (Garamycin) due to crystalline particles found during clarity testing at 24 months. This may cause eye injury if used.
9 recalls from H J Harkins Company Inc dba Pharma Pac are on record with U.S. safety agencies, from 2018–2020.
H J Harkins Company Inc dba Pharma Pac recalls Acetaminophen and Codeine Phosphate 300/30 mg tablet, packaged in: a) 10-count bottle (NDC 52959-0003-10), b) 12-count, dated Apr 15, 2020. Every H J Harkins Company Inc dba Pharma Pac recall is listed on this page, newest first.
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
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