Pfizer Inc. recalls Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only,…
Presence of Particulate Matter: Glass particulate matter detected in injectable.
Read the official notice →- Date
- 2023-02-01
- Country
- United States
- Brand
- Pfizer
- Product
- Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only,…
- Classification
- Class I
- Units
- USA nationwide and Puerto Rico
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Pfizer recalls
- 2024-01-24
US
Pfizer Inc. recalls 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL…
Presence of Particulate Matter; identified as glass
- 2023-11-15
US
Pfizer Inc. recalls 2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and injector per carton, Rx…
Presence of Particulate Matter: identified as glass.
FDA · DrugPfizer Inc.Nationwide in the US and Puerto Rico. The products were not distributed to…Official notice →- 2023-04-19
US
Pfizer Inc. recalls MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma Inc., a wholly owned subsidiary of Pfizer…
Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle labels state an expiry date of March 2026; the correct expiration date is February 2025.
- 2023-01-11
US
Pfizer Inc. recalls Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case (NDC…
Lack of assurance of sterility: Bags have the potential to leak.
- 2022-10-12
US
Pfizer Inc. recalls Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distributed by Hospira, Inc. Lake Forest, IL…
Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial.
- 2022-09-21
US
Other drugs & medical recalls in the United States
- 2023-02-01
US
Siemens Medical Solutions USA, Inc recalls Software : myNeedle Guide 2D license, myNeedle Guide 2D AWP only Workflow license, or myNeedle Guide 3D license. Used on the…
In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order of the orientation labels head , center, and feet in the axial thick slice segments are erroneously swapped
US
Getinge Usa Sales Inc recalls Getinge Flow-e Anesthesia System, Part No. 6887900
Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. If gas delivery is stopped, a sustained decrease in delivered O2 concentration may lead to hypoventilation and…
FDA · DeviceGetinge Usa Sales IncUS nationwide and Worldwide Distribution: Domestic distribution to AL, AR, AZ,…Official notice →US
Pharmacy Innovations recalls GLUTATHIONE L REDUCED 100MG/ML (2ML NEBVL) INHALATION; GLUTATHIONE L REDUCED 200MG/ML (1ML NEBVL) INHALATION; GLUTATHIONE L REDUCED…
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
US
Glaxosmithkline Consumer Healthcare Holdings DBA Haleon recalls Advil Liqui Gels (minis), Solubilized ibuprofen capsules, 200mg, Pain Reliever Fever Reducer (NSAID),…
Labeling: Illegible Label; the adhesive migrated onto a portion of the label, causing it to tear when peeled back
FDA · DrugGlaxosmithkline Consumer Healthcare Holdings DBA HaleonNationwide in the USA.Official notice →US
Spectrum Laboratory Products, Inc. recalls Epinephrine (L-Adrenaline), USP, CAS 51-43-4, 1 KG amber glass bottle in a vacuum sealed pouch, Rx only, Repackaged by…
Discoloration: Product complaints of the repackaged Epinephrine API being discolored which could result in less effective product
FDA · DrugSpectrum Laboratory Products, Inc.Nationwide in the USA, Puerto Rico and CanadaOfficial notice →US
Nephron Sc Inc recalls 0.9% Sodium Chloride Injection, USP, 100 mL Single-Dose Container bag, Rx Only, Nephron Pharmaceuticals Corporation, 4500 12th St.…
CGMP Deviations: potential for trace amounts of product carryover.