Recall Atlas
Drugs & medical

Spectrum Brands Pet Care Recalls Pet Fur deShedding Conditioner Due to Risk of Exposure to Bacteria

The recalled conditioner can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed…

Read the official notice → FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon)
Date
2024-06-06
Country
United States
Product
FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon)
Units
About 102,000 (In addition, about 250 were sold in Canada)
Category
Drugs & medical
Source
CPSC

Copied automatically from the US Consumer Product Safety Commission. Details may be shortened or out of date; the official notice is the authoritative source.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 Consumer Product Safety Commission has the exact models, batch codes and remedy, and it takes priority.

Other drugs & medical recalls in the United States

  1. 2024-06-12
  2. US
    Drugs & medicalClass III

    Bryant Ranch Prepack, Inc. recalls Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 200mL (when mixed), Each contains: cephalexin monohydrate, USP…

    Labeling: Not Elsewhere Classified: Back label states Each contains: cephalexin monohydrate, USP equivalent to 2.5g' instead of Each Bottle contains: cephalexin monohydrate, USP equivalent to 5g

    FDA · DrugBryant Ranch Prepack, Inc.Nationwide in the USAOfficial notice →
  3. US
    Drugs & medicalClass III

    Bryant Ranch Prepack, Inc. recalls Cephalexin for Oral Suspension, USP, 125mg per 5mL, Rx only, 100 Tablets, Relabeled by: Bryant Ranch Prepack, Inc, Burbank, CA 91504,…

    Labeling: Not Elsewhere Classified: Front label states 100 Tablets instead of 100 ml and on the back label 'Each Tablet contains' instead of 'Each Bottle contains' No total dose per bottle listed should be 2.5 g'

    FDA · DrugBryant Ranch Prepack, Inc.Nationwide in the USAOfficial notice →
  4. US
    Drugs & medicalClass II

    Glenmark Pharmaceuticals Inc., USA recalls Rizatriptan Benzoate Orally Disintegrating Tablets, USP 10mg, 18 (3 x 6) Unit-Dose Tablets, Manufactured for: Glenmark…

    CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are above the FDA acceptable limit.

    FDA · DrugGlenmark Pharmaceuticals Inc., USAUS Nationwide.Official notice →
  5. 2024-06-05
  6. US
    Drugs & medicalClass II

    Reflexion Medical, Inc. recalls RefleXion X1 Radiotherapy System Model RXM1000 Software version 2.1.19-3 Radiation therapy system is a device that combines the…

    A potential dose error exists for patients treated with an out of session SCINTIX partial fraction.

    FDA · DeviceReflexion Medical, Inc.U.S.: CA, CT, NJ, OR, PA and TX No O.U.S.Official notice →
  7. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls BD Pyxis(TM) Anesthesia Station 4000, REF: 338

    Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.

    FDA · DeviceCareFusion 303, Inc.Worldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
  8. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of…

    Potential for pressure wave data synchronization from two devices may not be correct.

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide distribution - US Nationwide in the states of CA, IN, OR and the…Official notice →
See all drugs & medical recalls →