Home › D. O. WEAVER AND COMPANY › Ten20 Conductive Paste
Ten20 Conductive Paste
D. O. WEAVER AND COMPANY · Model 10-20-4 · UDI-DI 00891893002222
GYB
Prescription
10
510(k) clearances
138
Adverse events (1 deaths)
10
Recalls
58
Facilities
Description
Single 4oz jar of Ten20 Conductive Paste (unit of use).
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-03-22 | Parker Laboratories, Inc. | Product demonstrates low viscosity. |
| 2024-02-07 | Natus Neurology Inc | Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Numb |
| 2024-02-07 | Natus Neurology Inc | Natus has become aware that its third-party supplier Parker Laboratories Inc. is conducting a voluntary recall related to their Tensive Conductive Adhesive Gel, Ref. 22-60 Lot Numb |
| 2024-01-22 | Parker Laboratories, Inc. | Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60. |
| 2021-08-24 | National Distribution & Contracting Inc | Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. |
| 2019-06-19 | Pharmaceutical Innovations, Inc. | Potential for failed stability antimicrobial effectiveness testing. |
| 2019-06-19 | Pharmaceutical Innovations, Inc. | Potential for failed stability antimicrobial effectiveness testing. |
| 2019-06-19 | Pharmaceutical Innovations, Inc. | Potential for failed stability antimicrobial effectiveness testing. |
| 2019-06-19 | Pharmaceutical Innovations, Inc. | Potential for failed stability antimicrobial effectiveness testing. |
| 2019-06-19 | Pharmaceutical Innovations, Inc. | Potential for failed stability antimicrobial effectiveness testing. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.