Pharmaceutical Innovations, Inc. recalls
Every recall we track for Pharmaceutical Innovations, Inc. — 6 in all, from 2019–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Pharmaceutical Innovations, Inc. peaked in 2019 (5); 6 since 2017.
All FDA recall records for Pharmaceutical Innovations, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 5 | 0 | 5 |
| 2020 | 0 | 0 | 0 | 1 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Pharmaceutical Innovations, Inc. recalls
What to do if you have a recalled Pharmaceutical Innovations, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Pharmaceutical Innovations, Inc. recalls
2 shown- UnratedMedical device
Pharmaceutical Innovations, Inc. recalls Ultra/Phonic Focus BP Conforming Gel Pads, UDI 00300361301021 (Primary); 10300361301028 (Package) - Product Usage: A
Pharmaceutical Innovations recalls Ultra/Phonic Focus BP Conforming Gel Pads due to FDA classification error; these pads are used during ultrasound exams for patient comfort and nipple location.
Pharmaceutical InnovationsAug 13, 2020 - Lower riskMedical device
Pharmaceutical Innovations, Inc. recalls ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.
Pharmaceutical Innovations recalls ElectroMist electrode conductivity spray solution (product codes 36-3310-25) due to potential failure in antimicrobial effectiveness testing. Affected units include specific lot numbers from 2014-2018.
Pharmaceutical InnovationsJun 19, 2019
Pharmaceutical Innovations, Inc. recall questions
How many recalls has Pharmaceutical Innovations, Inc. had?
6 recalls from Pharmaceutical Innovations, Inc. are on record with U.S. safety agencies, from 2019–2020.
What is the most recent Pharmaceutical Innovations, Inc. recall?
Pharmaceutical Innovations, Inc. recalls Ultra/Phonic Focus BP Conforming Gel Pads, UDI 00300361301021 (Primary); 10300361301028 (Package) - Product Usage: A, dated Aug 13, 2020. Every Pharmaceutical Innovations, Inc. recall is listed on this page, newest first.
Why are Pharmaceutical Innovations, Inc. products recalled?
The most common reasons on record: Potential for failed stability antimicrobial effectiveness testing. (5).
What should I do if I have a recalled Pharmaceutical Innovations, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Pharmaceutical Innovations, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.