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Alert: Akorn PrednisoLONE oral solution (15 mg/5mL, 240 mL bottles)
Akorn recalls one lot of PrednisoLONE oral solution (15 mg/5mL, 240 mL bottles) due to defective containers.
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Alert: Alaris infusion pumps
Becton Dickinson (BD)/Carefusion 303 recalls Alaris infusion pumps due to compatibility issues with Cardinal Health Monoject syringes. Use of…
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Alert: All ranitidine products (Zantac)
FDA requests removal of all ranitidine products (Zantac) from the market due to contamination with N-Nitrosodimethylamine (NDMA).
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Alert: Altaire Pharmaceuticals, Inc. recalls Perrigo brand ophthalmic products
Concerns about quality assurance controls
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Alert: American Health Packaging Valsartan Tablets, USP, 160 mg
Presence of probable human carcinogen N-Nitrosodiethylamine
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Alert: Amlodipine Valsartan Tablets USP, Valsartan HCTZ Tablets, USP and Valsartan Tablets USP
Presence of probable human carcinogen N-nitrosodiethylamine
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Alert: Amlodipine and Valsartan Tablets, USP; Valsartan Tablets, USP; and Valsartan and Hydrochlorothiazide Tablets, USP
Presence of probable carcinogen N-nitrosodiethylamine
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Alert: Amlodipine/Valsartan Combination Tablets and Amlodipine/Valsartan/Hydrochlorothiazide Combination Tablets
Presence above specification limits of probable carcinogen N-nitroso-diethylamine
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Alert: Ark Naturals Brushless Toothpaste Value Packs
Ark Naturals Brushless Toothpaste Value Packs recalled due to the potential for mold at some point during the product’s shelf life.
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Alert: Arrow MAC Two-Lumen Central Venous Access Kits
Teleflex and their subsidiary Arrow International, LLC recall Arrow MAC Two-Lumen Central Venous Access Kits and Arrow Pressure Injectable Arrowg+ard…
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Alert: Aurobindo Pharma/ScieGen Pharmaceuticals Irbesartan
Presence of probable carcinogen N-nitrosodiethylamine
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Alert: Aurobindo Pharma mirtazapine tablets
Aurobindo Pharma USA, Inc. recalls mirtazapine tablets due to a label error on declared strength.
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Alert: Aurobindo Quinapril and Hydrochlorothiazide Tablets USP 20mg/12.5mg
Aurobindo Pharma USA, Inc. recalls two lots of Quinapril and Hydrochlorothiazide Tablets USP 20mg / 12.5mg, due to presence of Nitrosamine Drug…
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Alert: AurobindoPharma Amlodipine Valsartan Tablets USP and Valsartan Tablets, USP (Expanded Recall)
Due to presence of probable carcinogen N-nitrosodiethylamine
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Alert: AurobindoPharma Acetris Valsartan Tablets, USP
Due to presence of probable carcinogen N-nitrosodiethylamine
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Alert: AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial
Eugia US LLC recalls lot number AC22006 of AuroMedics Acyclovir Sodium Injection 500 mg per 10 mL (50 mg/mL), 10 mL single dose vial due to a…
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Alert: IV bags containing fentanyl or oxytocin & various prefilled syringes
Nephron Sterile Compounding Center recalls 2.1 million doses of medicine and medical equipment due to a lack of assurance of sterility.
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Alert: Banamine transdermal (flunixin transdermal solution)
Intervet, Inc banamine transdermal (flunixin transdermal solution) recalled due to leakage between the cap and bottle.
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Alert: Banamine® (flunixin meglumine injection)
Merck Animal Health recalls three batches of BANAMINE®/BANAMINE®-S (flunixin meglumine injection) 50 mg/mL due to the presence of particulate matter.
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Alert: Banamine® (flunixin meglumine injection) expanded recall
Merck Animal Health recalls four additional batches of BANAMINE®/BANAMINE®-S (flunixin meglumine injection) 50 mg/mL due to the presence of…
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Alert: Baxter Clearlink Basic Solution Set with Duovent
Baxter Healthcare recalls over half a million Clearlink Basic Solution Sets with Duovent (used for chemotherapy) due to a risk of leaks that may…
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Alert: Baxter DiscPac Syringe Tip Caps
Baxter recalls certain packages of DiscPac Syringe Tip Caps, Self-Righting, Luer Slip, because of the potential for the packaging to fail to maintain…
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Alert: Baxter Healthcare Corporation Novum IQ Syringe infusion system
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple…
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Alert: B. Braun Medical Inc. blood administration sets
B. Braun Medical Inc. blood administration sets recalled due to potential leakage at joint between blood filter and tubing.