Pharmacy News

September 8, 2017

• Prescription Antibiotic Recalled – Morton Grove Pharmaceuticals Inc. is recalling 7332 bottles of amoxicillin and clavulanate potassium for oral suspension, USP, 250/62.5 mg per 5 mL, 100 mL when reconstituted (NDC 60432-065-00).

September 7, 2017

• Nationwide Opioid Recall – The possibility of leaky containers has prompted Tris Pharma Inc. to voluntarily recall morphine sulfate oral solution, 100 mg/5 mL (20 mg/mL) (NDC 27808-082-01).

August 15, 2017

• Seizure Medication Recalled – A labeling mix-up has prompted Precision Dose Inc. to voluntarily recall carbamazepine oral suspension, USP, 100 mg/5 mL, 5-mL unit dose cups (NDC 68094-301-59).

August 15, 2017

• Antibiotic Recall Active – Sterility concerns have prompted SCA Pharmaceuticals to recall cefazolin 3 g added to 100 mL 0.9% sodium chloride, total approximate volume 115 mL, single-dose container bags (NDC 70004-0524-32).

August 9, 2017

• International Laboratories, LLC Issues Voluntary Nationwide Recall of One (1) Lot of Pravastatin Sodium Tablets USP, 40mg Packaged in Bottles of 30 Tablets Due to Mislabeling NDC # 54458-925-16; Lot # 115698A.

August 9, 2017

• SCA Pharmaceuticals is recalling hydromorphone 0.5 mg/mL in 0.9% sodium chloride 1-mL fill in 3-mL Becton Dickinson syringe (NDC 70004-0302-05), due to lack of assurance of sterility; product has the potential to leak.

July 28, 2017

• Cyclobenzaprine HCl and Amantadine HCl by Apace Packaging: Recall – Potential Mislabeling

June 15, 2017

• Teva Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One Lot of Paliperidone Extended-Release Tablets, 3mg, 90 Count Bottles Distributed Under the Actavis Pharma Inc. Label Due to Dissolution Test Failure

June 14, 2017

• Topical Products by Phillips Company: Recall – Due to Concerns of Manufacturing Practices

June 10, 2017

• Bristol-Myers Squibb Voluntarily Recalls One Lot of Eliquis (apixaban) 5 mg Tablets

May 26, 2017

• Brilinta (ticagrelor) 90 mg tablets, 8-count Physician Sample Bottles: Recall of Lot # JB5047 – Due to Report of Another Medicine in One Bottle

May 25, 2017

• Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas™ 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information

April 21, 2017

• Phenobarbital 15 mg Tablets, USP by C.O. Truxton: Recall – Labeling Error on Declared Strength

April 4, 2017

• GSK recalling nearly 600,000 Ventolin inhalers in U.S.

March 31, 2017

• FDA alerts consumers of nationwide voluntary recall of EpiPen and EpiPen Jr

January 18, 2017

• Injectionn for Infants Recalled: 10% Premasol sulfite-free (Amino Acid) Injection, 2000 mL bulk package, Rx only

January 17, 2017

• Gastrointestinal Stimulant Recalled: Tri-Coast Pharmacy, Dexpanthenol 250 mg/mL (30 ML)

January 13, 2017

• Soluble Vitamin Recalled: Tri-Coast Pharmacy, Ascorbic Acid 500 mg/mL (50 ML)

January 13, 2017

• Prostaglandin Recalled: Alprostadil 20 mcg/mL Injectable vials. The ongoing, Class II recall affects both 5-mL and 10-mL vials distributed throughout the United States

January 13, 2017

• Decongestant Recalled: Wells Pharmacy Network LLC issued a nationwide recall of nearly 2000 5-mL vials of Phenylephrine HCl Injectable, 1 mg/mL (0.1%)

January 11, 2017

• Multivitamin IV Recalled

January 9, 2017

• Antifungal Injection Recalled

January 6, 2017

• Class I Recall of Dietary Supplement

January 5, 2017

• Anti-Cancer Medication Recalled

January 4, 2017

• Class I Recall of Constipation Med.

January 2, 2017

• Paralytic Drug Recalled.

December 28, 2016

• Narcotic Injection Recalled.

December 22, 2016

• Anticoagulant Recalled: Cantrell Drug Company is recalling 1494 syringes of Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride.

December 16, 2016

• Erectile Dysfunction Injection Recalled: Fallon Wellness Pharmacy, LLC, is recalling 10 1-mL vials of PAPA/PHEN/PROST (papaverine/phentolamine/prostaglandin) 18 mg/0.6 mg/0.006 mg/mL Injection.

December 11, 2016

• Antiemetic Drug Recalled – India-based drug manufacturer Cadila Pharmaceuticals Limited has recalled 6 kg of its Ondansetron HCL API,

December 9, 2016

• Diabetes Medication Recalled – Ascend Laboratories LLC is recalling 1739 1000-count bottles of Metformin Hydrochloride Tablets, USP 500 mg, due to the presence of foreign tablets.

November 10, 2016

• Muscle Relaxer Recall – PharMEDium Services, LLC, initiated a nationwide recall of succinylcholine chloride, 20 mg/mL, 200 mg/10 mL, 10-mL vials.

October 5, 2016

• Lansoprazole Recalled

September 28, 2016

• SSRI Recalled

September 16, 2016

• Virtus Pharmaceuticals Opco II, LLC Issues Voluntary Nationwide Recall of Hyoscyamine sulfate Due to Superpotent and Subpotent Results

September 14, 2016

• Selegiline Recalled

September 14, 2016

• ADHD Medication Recalled

September 8, 2016

• Novo Nordisk Inc. issues voluntary nationwide recall of six batches of GlucaGen® HypoKit® (glucagon [rDNA origin] for injection) due to detached needles on the syringe in the kit

August 4, 2016

• Seizure Medication Recalled: Divalproex sodium delayed-release tablets, USP, 250 mg., failed specifications

July 28, 2016

• Acetaminophen Overdose Antidote Recalled

July 22, 2016

• 35 Lots of Antidepressant Capsules Recalled

July 16, 2016

• Oral Liquid Docusate Sodium by PharmaTech: Recall – Contaminated with B. Cepacia

May 18, 2016

• Dr. Reddy’s recalls 50,000 bottles of Ondansetron tablets in US

April 26, 2016

• Prescription Coverage to Treat Hepatitis C Update: We updated our medical necessity criteria for coverage of Hepatitis C treatment and you may now be eligible for coverage. Under our revised policy, we will no longer restrict coverage based upon fibrosis levels.

March 28, 2016

• Compounded Products by Reliable Drug Pharmacy: Recall – Potential for Mislabeling and Lack of Quality Assurance

March 21, 2016

• Recall: Sodium Bicarbonate Injection, USP by Hospira: Recall – Particulate Matter

March 9, 2016

• Teva Pharmaceuticals Initiates Voluntary Nationwide Recall of One Lot of Amikacin Sulfate Injection USP 1 gram/4mL (250 mg/mL) Vials Due to Glass Particulate Matter

March 7, 2016

• Recall: Fluconazole Injection, USP, (in 0.9 Percent Sodium Chloride) 200mg per 100ml: Recall – Elevated Impurity

February 17, 2016

• Morphine Sulfate 0.5 mg/mL Preservative Free in 0.9 percent Sodium Chloride by Pharmakon Pharmaceuticals: Recall – Super-potent Product

January 11, 2016

• Perrigo Initiates Voluntary Product Recall in the U.S. Of Children’s Guaifenesin Grape Liquid and Guaifenesin DM Cherry Liquid Due to a Potential Defect with the Dosage Cup

October 30, 2015

• Sanofi US Issues Voluntary Nationwide Recall of ALL Auvi‑Q® Due to Potential Inaccurate Dosage Delivery

August 24, 2015

• Allergan Issues Voluntary Nationwide Recall In The U.S. Of Specific Lots Of REFRESH® Lacri-Lube®, REFRESH P.M. ®, FML® (fluorometholone ophthalmic ointment) 0.1%, and Blephamide® (Sulfacetamide Sodium And Prednisolone Acetate Ophthalmic Ointment, USP) 10%/0.2% For Particulate Matter

August 18, 2015

• Merck Recalls Temodar® and Temozolomide Capsules (generic) Bottles with Cracked Caps in the U.S. Due to Failure to Meet Child-Resistant Closure Requirement

August 4, 2015

• Hydrochlorothiazide Tablets by Unichem Pharmaceuticals (USA), Inc: Recall – Potential Presence of Foreign Tablets Contamination

May 5, 2015

• Recall: Adrucil (fluorouracil Injection, USP) 5 g/100 mL (50 mg/mL) – Particulate Matter

April 23, 2015

• Mylan Initiates Voluntary Nationwide Recall of Select Lots of Injectable Products Due to the Presence of Particulate Matter

April 9, 2015

• Baxter Initiates Voluntary Recall of Select Lots of IV Solutions Due to the Potential Presence of Particulate Matter

November 21, 2014

• Aurobindo Pharma USA, Inc. Issues Voluntary Nationwide Recall of Northstar Label Gabapentin Capsules, USP 300 mg Due to Complaints of Empty Capsules

October 31, 2014

• 10 Percent Neutral Buffered Formalin by Richard-Allan Scientific: Class I Recall – May Contain Incorrect Concentration of Formalin

October 20, 2014

• Kaiser Permanente® Issues Voluntary  Recall of Venlafaxine 37.5 mg ER tablets Manufactured by Sun  Pharmaceuticals, LTD

October 22, 2014

• Assured Brand Naproxen Sodium Tablets by Contract Packaging Resources, Inc.: Recall – Packaging Mix-Up

October 3, 2014

• Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Three Lots of Ketorolac Tromethamine Injection, USP, 30mg/ml Due to Labeling the Product with the Incorrect Expiration Date

April 2014

• First Time Generics (PDF)

March 6, 2014

• Pfizer Initiates Nationwide Voluntary Recall of Two Lots of Pfizer’s Effexor XR® 150 Mg Extended-Release Capsules and One Lot of Greenstone’s Venlafaxine HCl 150 Mg Extended-Release Capsules Due to the Possible Presence of Tikosyn® Capsules

January 17, 2013

• Advance Pharmaceutical Issues Nationwide Voluntary recall of one Lot (# 12G468) of Ferrous Sulfate Tablets, 325 mg, that may actually contain Meclizine HCl 25 mg tablets