Drugs & medicalClass II

Dr. Reddy's Laboratories, Inc. recalls Tacrolimus Capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Mfd. by Dr. Reddy's Laboratories Limited, Bachupally - 500 090,…

Presence of Foreign Tablets/Capsules: Presence of one Tacrolimus 1 mg capsule co-mingled in a bottle containing and labeled as Tacrolimus 0.5 mg capsules.

Read the official notice →
Date
2023-03-01
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Tacrolimus Capsules, USP, 0.5 mg, 100-count bottle, Rx Only, Mfd. by Dr. Reddy's Laboratories Limited, Bachupally - 500 090, INDIA; NDC…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Dr. Reddy's Laboratories recalls

  1. 2024-01-17
  2. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Tacrolimus Capsules, USP 1mg, 100-Count Bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories Limited, Bachupally, 500 090,…

    Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in a bottle of 1 mg Tacrolimus capsules.

    FDA · DrugDr. Reddy's Laboratories, Inc.US Nationwide.Official notice →
  3. 2023-11-15
  4. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Montelukast Sodium Tablets, USP 10 mg, Rx Only, 1000 count bottle, Distributed by: Dr. Reddy's Laboratories., Princeton, NJ…

    Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was found in a bottle of Montelukast Sodium Tablets, USP 10mg, identified as metoprolol 25 mg.

    FDA · DrugDr. Reddy's Laboratories, Inc.NationwideOfficial notice →
  5. 2023-07-26
  6. US
    Drugs & medicalClass II

    Dr Reddy's Laboratories Limited recalls Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Srikakulam - 532 409…

    Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.

    FDA · DrugDr Reddy's Laboratories LimitedNationwide in the USAOfficial notice →
  7. 2022-12-07
  8. US
  9. 2022-10-12
  10. 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 →
  11. 2022-08-03
  12. US
All 35 Dr. Reddy's Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2023-03-01
  2. US
    Drugs & medicalClass II

    RISING PHARMACEUTICALS recalls Warfarin Sodium Tablets, USP 1 mg, 100-count bottle, Rx Only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC# 57237-119-01

    Failed Impurities/Degradation Specifications

    FDA · DrugRISING PHARMACEUTICALSProduct was distributed to 16 distributors and 8 wholesalers who may have…Official notice →
  3. 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 →
  4. US
  5. US
    Drugs & medicalClass III

    Advantice Health, Llc recalls Dermoplast FIRST AID ANTIBACTERIAL SPRAY (Benzethonium chloride 0.2% First aid antiseptic, Benzocaine 20%) Topical analgesic, NET WT. 2.75…

    Subpotent Drug: Low assay observed in one of the two active ingredients during stability testing.

    FDA · DrugAdvantice Health, LlcProduct was distributed via the internet, distributors and retailers nationwide.Official notice →
  6. 2023-02-22
  7. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc. recalls SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R…

    This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

    FDA · DeviceSiemens Medical Solutions USA, Inc.Worldwide distribution - US Nationwide and the countries of Japan, Chile,…Official notice →
  8. US
    Drugs & medicalClass II

    Conformis, Inc. recalls iTotal Identity Impactor Handle, Model No. 1080-212/ED-07827 REV AE

    Loctite thread locker (epoxy) may not have been applied to the screw that is part of the handle. In the absence of epoxy, the screw may loosen and fall into the patient during a procedure.

    FDA · DeviceConformis, Inc.US Nationwide distribution in the states of AL, AZ, CO, FL, GA, KS, KY, LA,…Official notice →
See all drugs & medical recalls →