ZOLL Pro-padz Liquid Gel Radiolucent — Class II medical device recall Z-1945-2019
Terminated recall by Bio-Detek, Inc., reported 2019-07-10, distributed in AZ, CA, CO, CT, FL, LA, MN, NV…. Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing th
| Recall number | Z-1945-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bio-Detek, Inc., Pawtucket, RI, United States |
| Recall initiated | 2019-05-28 |
| Classified | 2019-07-03 |
| Reported by FDA | 2019-07-10 |
| Terminated | 2020-06-01 |
| Distributed | AZ, CA, CO, CT, FL, LA, MN, NV, OH, PA, TN, UT, WY |
| Countries outside the US | CA, DE, FR, IT |
| Quantity | 1,789 |
| NDC | 08900-2105-01, 08900-2106-01 |
| Lot numbers | 1719, 1719A, 1819 |
| Model numbers | 8900-2105-01 |
Product
ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)
Reason for recall
Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1945-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.