Drugs & medicalClass III

The Ritedose Corporation recalls 23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx Only, RITEDOSE, 503B Outsourcing Facility, A…

Labeling: Incorrect Barcode: Product barcode incorrectly identifies the product as rocuronium bromide injection 100 mg per 10 mL instead of sodium chloride injection 23.4%, 120 mEq per 30 mL.

Read the official notice →
Date
2022-04-13
Country
United States
Brand
Ritedose
Product
23.4% Sodium Chloride Injection, 120 mEq per 30 mL (4 mEq/mL), 50 mL prefilled syring, Rx Only, RITEDOSE, 503B Outsourcing Facility, A…
Classification
Class III
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Ritedose recalls

  1. 2023-08-09
  2. US
    Drugs & medicalClass II

    The Ritedose Corporation recalls Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation…

    CGMP deviation: product released prior to supplier approval.

    FDA · DrugThe Ritedose CorporationNationwide in the USOfficial notice →
All 2 Ritedose recalls →

Other drugs & medical recalls in the United States

  1. 2022-04-13
  2. US
    Drugs & medicalClass II

    Mylan Pharmaceuticals Inc recalls Travoprost Ophthalmic Solution, USP, 0.004%, 2.5 mL bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV…

    Subpotent Drug and Failed Impurities/Degradation Specifications: low out-of-specification results obtained for assay and high out-of-specification results for related substance impurities/degradation during routine…

    FDA · DrugMylan Pharmaceuticals IncNationwide in the USA and Puerto RicoOfficial notice →
  3. US
    Drugs & medicalClass III

    Advanced Accelerator Applications USA, Inc. recalls NETSPOT (kit for the preparation of Ga 68 dotatate injection) 40 mcg dotatate, kit contains Vial 1 (Reaction vial…

    Subpotent Drug: low out-of-specification results for Vial 1 assay obtained during stability studies.

    FDA · DrugAdvanced Accelerator Applications USA, Inc.Nationwide in the USA and Puerto RicoOfficial notice →
  4. US
    Drugs & medicalClass II

    MERCK SHARP & DOHME CORP recalls Janumet (sitagliptin and metformin HCl) tablets, 50 mg/500 mg, 14-count bottle, packaged as 2 bottles per carton , Sample-Not For Sale,…

    Presence of foreign substance: Presence of stainless steel particulates in tablets.

    FDA · DrugMERCK SHARP & DOHME CORPNationwide in the USAOfficial notice →
  5. US
    Drugs & medicalClass II

    Vitae Enim Vitae Scientific, Inc. recalls TETRACAINE 1% Tetracaine HCI Injection, USP, 20mg/2mL (10mg/mL), 10 x 2ml Single Use Vials per box, Rx only, Manufactured for…

    Lack of Assurance of Sterility: deviations from Current Good Manufacturing Practices (CGMP) that call into question the sterility of products intended to be sterile.

    FDA · DrugVitae Enim Vitae Scientific, Inc.Nationwide in the U.S.AOfficial notice →
  6. 2022-04-06
  7. US
    Drugs & medicalClass II

    Medtronic MiniMed recalls MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781,…

    New or replacement insulin pumps are not pre-programmed with basal rates or other verified settings (bolus wizard settings, sensor settings, etc.), which must be set up and saved on pumps prior to use. Patients who do…

    FDA · DeviceMedtronic MiniMedUS: OH, UT, IL, NY, FL, LA, NE, NV, CA, VA, TX, DE, KS, MS, MI, AL, OK, AZ,…Official notice →
  8. US
    Drugs & medicalClass II

    Illumina, Inc. recalls Illumina NextSeq 550Dx, REF: 20005715, CE, IVD

    There is a potential that the DNA sequence analyzer may short circuit shortly after disconnection and reconnection of circuit board or imaging module due to an insufficient reconnection of the ribbon cable. The short…

    FDA · DeviceIllumina, Inc.US: PA, WA, CA, MI, FL, MD, AR, UT NC, Fl, IL, NE, NJ, TN, NY, IN, CO, GA, OK,…Official notice →
See all drugs & medical recalls →