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.

Date

2022-10-12

Country

United States

Brand

Pfizer

Product

Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distributed by Hospira, Inc. Lake Forest, IL…

Classification

Class II

Units

Distributed in the United States 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 Details may be shortened or out of date; the official notice is the authoritative source.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

1. Check the product name, strength and lot number against the official notice.
2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
3. 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

1. 2023-04-19
2. US
   Drugs & medicalClass III

   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.

   FDA · DrugPfizer Inc.Nationwide in the USAOfficial notice →
3. 2023-02-01
4. US
   Drugs & medicalClass I

   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.

   FDA · DrugPfizer Inc.USA nationwide and Puerto RicoOfficial notice →
5. 2023-01-11
6. US
   Drugs & medicalClass II

   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.

   FDA · DrugPfizer Inc.Nationwide in the USA.Official notice →
7. 2022-09-21
8. US
   Drugs & medicalClass I

   Pfizer Inc. recalls PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray…

   Presence of particulate matter

   FDA · DrugPfizer Inc.USA NationwideOfficial notice →
9. 2022-08-03
10. US
    Drugs & medicalClass I

    Pfizer Inc. recalls Propofol Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL per glass fliptop vial (NDC 0409-4699-54) further packaged in a…

    Presence of particulate matter: particulate identified as a beetle.

    FDA · DrugPfizer Inc.USA NationwideOfficial notice →
11. 2022-05-25
12. US
    Drugs & medicalClass II

    Pfizer Inc. recalls Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

    CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.

    FDA · DrugPfizer Inc.Nationwide and Puerto RicoOfficial notice →

Other drugs & medical recalls in the United States

1. 2022-10-12
2. US
   Drugs & medicalClass II

   CIPLA recalls Arformoterol Tartrate Inhalation Solution, 15 mcg/2mL, 2 mL Sterile Unit-Dose Vial packaged in 5 x 2 mL Sterile Unit-Dose Vials per pouch,…

   Lack of Assurance of Sterility: environmental monitoring failure.

   FDA · DrugCIPLAProduct was distributed nationwide to distributors/wholesalers who may have…Official notice →
3. US
   Drugs & medicalClass III

   Dr. Reddy's Laboratories, Inc. recalls Phytonadione Injectable Emulsion USP, 10 mg/mL, 25x 1 mL single dose ampules per carton, Rx only, Distributed by: Dr. Reddy's…

   Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.

   FDA · DrugDr. Reddy's Laboratories, Inc.USA nationwideOfficial notice →
4. US
   Drugs & medicalClass III

   Woodbine Products Co Inc recalls Antibacterial Foaming Wash with Hydria Moisturizing Formula, Cucumber-Melon Scent, 1250 mL (42 fl oz.), Manufactured for: Triple S,…

   Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.

   FDA · DrugWoodbine Products Co IncNCOfficial notice →
5. US
   Drugs & medicalClass I

   Salon Technologies International Inc recalls Antica Farmacista Hand Sanitizer Ocean Citron (ethyl alcohol, denatured 65%) packaged in 473 mL/16 fl. oz. bottles, Dist.…

   Chemical Contamination: product found to contain benzene

   FDA · DrugSalon Technologies International IncFL and WA onlyOfficial notice →
6. US
   Drugs & medicalClass II

   Salon Technologies International Inc recalls Sanitizing Hand Spray 80% (alcohol 80% v/v) Packaged in 2 FL OZ (60 mL) bottles, Salon Technologies International 8810…

   GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

   FDA · DrugSalon Technologies International IncFL and WA onlyOfficial notice →
7. 2022-10-05
8. US
   Drugs & medicalClass II

   MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

   Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector is coming apart from the assembled device when pulling the catheter out of the artificial airway in the…

   FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldNationwide distribution to AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID,…Official notice →