Drugs & medicalClass III

Dr. Reddy's Laboratories, Inc. recalls Sirolimus Tablets 1mg Tablets 100-count bottle, Rx Only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made…

Failed Impurities/Degradation Specifications

Read the official notice →
Date
2024-05-29
Country
United States
Brand
Dr. Reddy's Laboratories
Product
Sirolimus Tablets 1mg Tablets 100-count bottle, Rx Only, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in…
Classification
Class III
Units
US Nationwide.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-07-10
  2. US
  3. US
    Drugs & medicalClass III

    Dr. Reddy's Laboratories, Inc. recalls Eszopiclone Tablets, USP 1mg CIV, 30-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090…

    Failed Impurities/Degradation Specifications: Related Substances

    FDA · DrugDr. Reddy's Laboratories, Inc.OH, MSOfficial notice →
  4. 2024-06-05
  5. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories…

    Lack of Assurance of Sterility: Leaking vials

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide within the United StatesOfficial notice →
  6. 2024-05-15
  7. US
    Drugs & medicalClass I

    Dr. Reddy's Laboratories, Inc. recalls Sapropterin Dihydrochloride Powder for Oral Solution 100mg, 30 individual packets per carton, Rx Only, Distributor: Dr. Reddy's…

    Sub-potent Drug; powder discoloration associated with decreased potency

    FDA · DrugDr. Reddy's Laboratories, Inc.Nationwide in the USAOfficial notice →
  8. 2024-02-14
  9. US
  10. 2024-01-17
  11. US
    Drugs & medicalClass II

    Dr. Reddy's Laboratories, Inc. recalls Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC…

    Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.

    FDA · DrugDr. Reddy's Laboratories, Inc.USA NationwideOfficial notice →
All 35 Dr. Reddy's Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2024-05-29
  2. US
    Drugs & medicalClass II

    American Regent, Inc. recalls Vasopressin Injection, USP, 200 Units per 10 mL (20 Units per mL), 10 mL Multiple-Dose Vial, Rx only, For Intravenous Infusion, American…

    Subpotent product in addition to having out-of-specification results for impurities.

    FDA · DrugAmerican Regent, Inc.USA NationwideOfficial notice →
  3. US
    Drugs & medicalClass II

    SOMERSET THERAPEUTICS LLC recalls Haloperidol decanoate Injection 50mg/mL, packaged in a) 1 mL Single-Dose Vials (NDC 70069-381-01) and b) 10 1mL Single-Dose Vials (NDC…

    Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).

    FDA · DrugSOMERSET THERAPEUTICS LLCNationwide within the United StatesOfficial notice →
  4. US
    Drugs & medicalClass II

    Preferred Pharmaceuticals, Inc. recalls Duloxetine Delayed-Release Cap USP 30mg, 30-count bottle, Rx only, Preferred Pharmaceutcals, Inc., NDC 68788-9301-03

    CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

    FDA · DrugPreferred Pharmaceuticals, Inc.Product distributed to CA, FL, OK, KS and CTOfficial notice →
  5. US
  6. US
    Drugs & medicalClass III

    SUN PHARMACEUTICAL INDUSTRIES INC recalls Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun Pharmaceutical…

    Failed Release Testing: Out of specification for particulate matter test.

    FDA · DrugSUN PHARMACEUTICAL INDUSTRIES INCTX, PAOfficial notice →
  7. 2024-05-22
  8. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic.

    Potential contamination of the product with latex adhesive residual.

    FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution.Official notice →
See all drugs & medical recalls →