Adverse Events and Recalls

The company is voluntarily recalling product due to particulate matter.

The company issues a voluntary nationwide recall due to the presence of particulate matter in a single vial.

The company is voluntarily recalling all unexpired lots of 50-mm, 0.2-micron filters.

Wells Pharmacy Network is voluntarily recalling all of its products due to sterility concerns.

Virtus Pharmaceuticals Opco II, LLC is voluntarily recalling batches of hyoscyamine sulfate (0.125mg).

The company voluntarily recalled the product due to detached needles on the syringe in the kit.

A customer complaint revealed microbial contamination issues affecting lots with expiration dates in late 2018 and early 2019.

The company is voluntarily recalling one lot of product due to a potential packaging mistake.

Arbor Pharmaceuticals is voluntarily recalling Cetylev (acetylcysteine) effervescent tablets due to inadequate seal of the blister pack.

The company is voluntarily recalling one lot of product due to particulate matter.

The company is voluntarily recalling liquid products due to possible Burkholderia cepacia contamination.

The company is voluntarily recalling a docusate sodium solution distributed by Rugby Laboratories due to risk of contamination.

The company recalls products due to sterility concerns.

The company voluntarily recalls product due to particulate matter.

The company has recalled one lot of 50% magnesium sulfate injection, USP due to particulates.

Hospira recalls one lot of 8.4% Sodium Bicarbonate Injection, USP, due to particulate matter found within a single-dose glass fliptop vial.

Both agencies warn of increased rates of serious adverse events, including death, during clinical trials of Zydelig (idelalisib).

The company recalls one lot of amikacin sulfate injection USP, 1 gram/4mL (250 mg/mL) vials due to the potential presence of glass particulate in one vial.

Sagent Pharmaceuticals issues a nationwide recall of Fluconazole injection, USP, due to out of specification impurity results.

Baxter has voluntarily recalled lots of IV solutions due to potential container leakages and particulate matter.

Abbott’s Compounding Pharmacy voluntarily recalls sterile products due to lack of sterility assurance.

The company has voluntarily recalled one lot of magnesium sulfate in water for injection because of incorrect labeling.

Baxter voluntarily recalls two lots of intravenous solutions due to particulates.

The company is voluntarily recalling the epinephrine injection, USP because of potential inaccurate dosage delivery.

US Compounding, Inc. issues voluntary recall of all sterile products.

Allergan issued a voluntary nationwide recall in the US of specific lots of ophthalmic ointment after customers complained of black particles, which came from the cap.

Baxter has recalled of one lot of IV solution due to the potential for leaking containers, particulate matter, and missing port.

Moses Lake Professional Pharmacy issues recall due to lack of sterility assurance.

The company voluntarily recalls select lots of Adrucil due to particulate matter.

Mylan announces a recall of eight lots of injectable products due to visible foreign particulate matter.