Find a dangerous drug or medical device lawyer in Tucson: call, report, save
If a medicine may be hurting you now, the Arizona Poison and Drug Information Center answers at 1-800-222-1222, free and in confidence, all day. You can report a serious reaction to the FDA yourself, and your doctor does not have to. A claim over a drug you took in Tucson follows the two-year injury statute for products.
Last checked November 9, 2026 · Official sources (25)
Who can you call in Tucson if a medicine may be hurting you?
Call the Arizona Poison and Drug Information Center at 1-800-222-1222. Calls cost nothing, stay private and are answered at any hour. The center is part of the University of Arizona College of Pharmacy.
Do not quit a medicine without a plan. Stopping suddenly can be more harmful. Talk to your prescriber or pharmacist first. In an emergency, Banner - University Medical Center Tucson has a state-designated Level I trauma center.
How do you report a bad reaction or a faulty device in Tucson?
| Problem | Where to report | Notes |
|---|---|---|
| Serious reaction or product problem | FDA MedWatch | Patients can use the online form themselves. |
| Your doctor will not report it | FDA MedWatch | Providers are not required to report, so you may need to. |
| A pharmacy filled it wrong | Arizona State Board of Pharmacy | Online complaint form |
| A prescriber's care | Arizona Medical Board | Toll free (877) 255-2212 |
A report is not a lawsuit, and it does not stop any deadline.
What should you save after a drug or device injury?
- Keep the bottle, packaging and label. Compare your lot number to any recall notice.
- Keep a removed device in a sealed bag. Ask the surgeon to keep it for you.
- Ask for pharmacy and prescribing records, including the warnings you were given.
- Request your Banner records through MRO Patient Central. Banner has 30 days to act on that request.
- Write down every symptom with dates, and every Tucson doctor or pharmacy you saw.
Can you sue a drug or device maker from Tucson?
| Product | What the law does |
|---|---|
| Brand drug | The maker is responsible for its label at all times. |
| Generic drug | Federal law requires generic labels to match the brand, and claims turning on warnings are preempted. |
| Premarket approved device | Common-law safety claims are barred. |
| FDA-approved drug, punitive damages | The maker is generally not liable, unless it knowingly withheld information from the FDA. |
| Vaccine | A no-fault federal program may apply. |
These rules cut some claims off and leave others. Which one fits your pill or device is a question for a lawyer, and it can decide the whole case.
Who pays the bills while a Tucson claim is pending?
Bills usually run through your health plan, Medicare or Medicaid. Medicare must be repaid from a settlement, and providers may have a lien on an injury recovery. Arizona's constitution bars caps on injury damages, but that is not a promise of any amount.
How long do you have to sue after a drug or device injury in Tucson?
For a claim from Tucson, generally 2 years, the product deadline following the injury statute. Write down the date you first learned the drug may have caused the harm. For a child it waits until age 18.
Questions
Should I stop taking my medicine?
Not suddenly. Stopping can be more harmful, so call your prescriber or the poison center first.
Does my doctor report my reaction to the FDA?
Not necessarily. A provider is not required to report, but you can.
Where do I file a complaint about a Tucson pharmacy?
With the Arizona State Board of Pharmacy, which takes online complaints.
Is there a limit on what I can recover in Arizona?
Arizona's constitution leaves no room for a cap on a Tucson drug injury award.
Dangerous drug or medical device in Tucson? See if you are owed money.
A free case review. $0 upfront. No fee unless you win.
See if I’m owed moneySources (25)
- Arizona Poison and Drug Information Center, checked 2026-11-09. “1-800-222-1222 - Free - Confidential 24 Hours a Day - 7 Days a Week”
- FDA MedWatch, checked 2026-11-09. “you may complete the Online Reporting Form yourself”
- FDA MedWatch, checked 2026-11-09. “Your health care provider is NOT required to report to the FDA.”
- A.R.S. 12-551, checked 2026-11-09. “shall be commenced and prosecuted within the period prescribed in section 12-542”
- Arizona Poison and Drug Information Center, Who We Are, checked 2026-11-09. “The Arizona Poison and Drug Information Center is a center of excellence at the University of Arizona College of Pharmacy.”
- FDA MedWatch, checked 2026-11-09. “program for reporting serious reactions, product quality problems”
- FDA, checked 2026-11-09. “stopping your medicine may be more harmful to your health than continuing to take the recalled medicine”
- FDA, checked 2026-11-09. “check the lot number on the label of your medicine”
- Arizona Constitution, art. 18, sec. 6, checked 2026-11-09. “the amount recovered shall not be subject to any statutory limitation”
- Arizona DHS, State Designated Trauma Centers, checked 2026-11-08. “1625 N. Campbell Ave, Tucson, AZ 85719 11/11/24 11/11/27”
- Arizona State Board of Pharmacy, checked 2026-11-09. “File a complaint or self report online with the Board of Pharmacy”
- Arizona Medical Board, Investigations, checked 2026-11-09. “instructions for how to file a complaint”
- Banner Health, Patient Medical Records, checked 2026-11-08. “you can request your medical records from any Banner Health hospital, provider office, or urgent care location.”
- 45 CFR 164.524, checked 2026-11-09. “no later than 30 days after receipt of the request”
- Supreme Court, Wyeth v. Levine (2009), checked 2026-11-09. “the manufacturer bears responsibility for the content of its label at all times”
- Supreme Court, PLIVA v. Mensing (2011), checked 2026-11-09. “violated the federal requirement that generic drug labels be the same as the corresponding brand-name drug labels”
- Supreme Court, Mutual Pharmaceutical v. Bartlett (2013), checked 2026-11-09. “State-law design-defect claims that turn on the adequacy of a drug's warnings are pre-empted by federal law under PLIVA.”
- Supreme Court, Riegel v. Medtronic (2008), checked 2026-11-09. “bars common-law claims challenging the safety or effectiveness of a medical device marketed in a form that received premarket approval from the FDA”
- A.R.S. 12-701, checked 2026-11-09. “is not liable for exemplary or punitive damages if the drug alleged to cause the harm”
- A.R.S. 12-701, checked 2026-11-09. “knowingly, in violation of applicable federal food and drug administration regulations, withheld from or misrepresented”
- HRSA, checked 2026-11-09. “is a no-fault alternative to the traditional legal system for resolving vaccine injury petitions”
- CMS, checked 2026-11-09. “it must be repaid to Medicare when a settlement, judgment, award, or other payment is made”
- A.R.S. § 33-931, checked 2026-11-09. “is entitled to a lien for the care and treatment or transportation of an injured person”
- A.R.S. § 12-542, checked 2026-11-08. “within two years after the cause of action accrues”
- A.R.S. § 12-502, checked 2026-11-08. “the period of such disability shall not be deemed a portion of the period limited for commencement of the action”