Drugs & medicalClass II

B. Braun Medical Inc recalls Heparin Sodium, 25,000 USP units per 250mL, (100 USP units per mL) in 5% Dextrose injection, 250 ml Excel Container, B. Braun Medical Inc.…

Subpotent: Low anti-factor IIa Potency.

Read the official notice →
Date
2023-05-24
Country
United States
Brand
B. Braun Medical
Product
Heparin Sodium, 25,000 USP units per 250mL, (100 USP units per mL) in 5% Dextrose injection, 250 ml Excel Container, B. Braun Medical Inc.…
Classification
Class II
Units
Nationwide in the USA
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 Details may be shortened or out of date; the official notice is the authoritative source.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 B. Braun Medical recalls

  1. 2023-08-16
  2. US
    Drugs & medicalClass III

    B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018, NDC 0264-5802-00

    Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.

    FDA · DrugB. Braun Medical Inc.United StatesOfficial notice →
  3. 2023-07-19
  4. US
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    B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA, NDC…

    Lack of assurance of sterility: bags have the potential to leak.

    FDA · DrugB. Braun Medical Inc.USA NationwideOfficial notice →
  5. 2023-07-05
  6. US
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    B. Braun Medical, Inc. recalls Design Options¿ / Epidural anesthesia kit (10 count carton)

    Kits were assembled with the incorrect Filter Straw.

    FDA · DeviceB. Braun Medical, Inc.US Nationwide distribution.Official notice →
  7. 2023-03-15
  8. US
  9. 2023-03-01
  10. US
    Drugs & medicalClass II

    B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection, USP, 500 mL Excel Plus Container, Rx Only, B. Braun Medical Inc. Bethlehem, PA 18018, NDC 0264-5802-10

    Lack of sterility assurance: Recall of certain batches of 0.9% Sodium Chloride for Injection USP in EXCEL¿ Plus IV Container product due to the possibility of an incomplete seal that may cause leakage. The impacted…

    FDA · DrugB. Braun Medical Inc.USA Nationwide.Official notice →
  11. 2022-12-14
  12. US
    Drugs & medicalClass II

    B. Braun Medical, Inc. recalls 0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc. Bethlehem, PA 18018-3524…

    Lack of sterility assurance: Bags have the potential to leak.

    FDA · DrugB. Braun Medical, Inc.FL, NJ, PAOfficial notice →
All 53 B. Braun Medical recalls →

Other drugs & medical recalls in the United States

  1. 2023-05-24
  2. US
    Drugs & medicalClass I

    Draeger Medical, Inc. recalls VentStar Basic (P)180, MP00351

    Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

    FDA · DeviceDraeger Medical, Inc.Domestic: US Nationwide Distribution.Official notice →
  3. US
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    Astral SteriTech Private Ltd. recalls Piperacillin and Tazobactam for Injection, USP 4.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC…

    Lack of Assurance of Sterility

    FDA · DrugAstral SteriTech Private Ltd.Nationwide within the United StatesOfficial notice →
  5. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Ketotifen Fumarate 0.025 %, Antihistamine eye drops, 5mL bottle, MFG: Akorn, Lake Forrest IL 60045, Repackaged by: RemedyRepack Inc.,…

    CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.

    FDA · DrugRemedyRepack Inc.Product was distrituded to three direct account in PA.Official notice →
  6. US
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    Sanofi-Aventis U.S. LLC recalls Admelog, insulin lispro injection, 100 units/mL (U-100), 3mL multi-dose vial, Rx Only, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807 A…

    Lack of Assurance of Sterility: Malformed crimped collar seal

    FDA · DrugSanofi-Aventis U.S. LLCNationwide in the USAOfficial notice →
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    Hikma Pharmaceuticals USA Inc. recalls Lorazepam Injection, USP, 2mg/mL, 1 mL vial (NDC 0641-6044-01), packaged in 25 x 1 mL Vials per carton (NDC 0641-6044-25), Rx…

    Failed Impurities/Degradation Specifications: Out-of-specification results for total related compounds observed during retain steting due to the elevated Related Compound-C.

    FDA · DrugHikma Pharmaceuticals USA Inc.Nationwide in the USA and Puerto RicoOfficial notice →
See all drugs & medical recalls →