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Mckesson Packaging Services Recalls
17 recalls on record · October 10, 2012 to May 2, 2018 · Drugs
Recalls by year
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18
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 2, 2018DrugsFDA
Mckesson Packaging Services recalls Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Rid
Hazard: Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
May 2, 2018DrugsFDA
Mckesson Packaging Services recalls Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actav
Hazard: Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
May 2, 2018DrugsFDA
Mckesson Packaging Services recalls Diltiazem HCl Extended-Release Capsules, USP 120 mg, 100-count bottles, Rx only, Mfg. By: Par Pharmaceutical One Ram Rid
Hazard: Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
March 14, 2018DrugsFDA
Mckesson Packaging Services recalls RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 1
Hazard: Failed Stability Specifications
February 14, 2018DrugsFDA
Mckesson Packaging Services recalls Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson Pack
Hazard: Subpotent Drug: Out of specification for assay (stability testing)
September 13, 2017DrugsFDA
Mckesson Packaging Services recalls Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By
Hazard: Failed moisture limits: Out of specification for moisture content.
July 5, 2017DrugsFDA
Mckesson Packaging Services recalls BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center
Hazard: Failed Moisture Limits: Product tested out-of-specification for moisture content.
May 3, 2017DrugsFDA
Mckesson Packaging Services recalls Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only, Manufacture
Hazard: Supotent: Out of Specification result for assay test during routine stability testing.
March 15, 2017DrugsFDA
Mckesson Packaging Services recalls Aspirin Chewable Tablets, 81 mg, (NSAID*), packaged in UD 750 Tablets (25 x 30) tablets in blisters per carton, Dist. By
Hazard: Presence of Foreign Substance: foreign material found in the bulk inventory.
October 5, 2016DrugsFDA
Mckesson Packaging Services recalls Lansoprazole Delayed-Release Capsules, USP, 30 mg, packaged in 100-count cartons of 10 x 10 unit dose blister cards, Rx
Hazard: Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole DR 40mg Capsules, but the outer secondary packaging was mislabeled Lansoprazole Delayed-Release 30mg Capsules.
October 5, 2016DrugsFDA
Mckesson Packaging Services recalls Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., P
Hazard: Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).
May 4, 2016DrugsFDA
Mckesson Packaging Services recalls SKY Aspirin Chewable Tablets, 81 mg, Unit Dose 750 tablets (25 x 30) box, OTC, Distributed by: McKesson Packaging Servic
Hazard: Labeling: Label mix-up -outer carton incorrectly labeled as aspirin chewable tablets.
August 13, 2014DrugsFDA
Mckesson Packaging Services recalls Alprazolam Tablets, USP 0.25 mg, UD 100 Tablets (10 x 10), Rx Only, Mfg By: Sandoz, Inc., Princeton, NJ 08540 --- NDC 63
Hazard: Presence of Foreign Substance; tablets may contain stainless steel metal particulates
August 6, 2014DrugsFDA
Mckesson Packaging Services recalls Aspirin DR Enteric Coated Tablets, USP 325 mg, UD 750 tablets (25x30), Dist. By: McKesson Packaging Services a business
Hazard: Failed Dissolution Specification; at the 12 month time interval.
March 26, 2014DrugsFDA
McKesson Packaging Services recalls Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by
Hazard: Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
October 10, 2012DrugsFDA
McKesson Packaging Services recalls buPROPion Hydrochloride Extended-Release Tablets (XL), 300 mg, UD 100 Tablets (10 x 10) per carton, Rx only, Mfg By: CMI
Hazard: Failed USP Dissolution Test Requirements: Possible out-of-specification dissolution results at the 8 hour stability testing point.
October 10, 2012DrugsFDA
McKesson Packaging Services recalls buPROPion Hydrochloride Extended-Release Tablets (XL), 150 mg, UD 100 Tablets (10 x 10) per carton, Rx only, Mfg By: CMI
Hazard: Failed USP Dissolution Test Requirements: Possible out-of-specification dissolution results at the 8 hour stability testing point.