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RALLY
Smith & Nephew, Inc. · Model 71271605 · UDI-DI 00885556646403
LOD
Prescription
1
510(k) clearances
13,179
Adverse events (469 deaths)
36
Recalls
82
Facilities
Description
RALLY HV ALL IN ONE SYSTEM 70 GRAMS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-20 | Heraeus Medical GmbH (Dental Division) | Potential for monomer liquid leakage. |
| 2026-08-20 | Heraeus Medical GmbH (Dental Division) | Potential for monomer liquid leakage. |
| 2025-12-09 | Heraeus Medical GmbH (Dental Division) | increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule b |
| 2025-12-09 | Heraeus Medical GmbH (Dental Division) | increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule b |
| 2025-12-09 | Heraeus Medical GmbH (Dental Division) | increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule b |
| 2025-12-09 | Heraeus Medical GmbH (Dental Division) | increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule b |
| 2022-11-07 | Howmedica Osteonics Corp. | Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is |
| 2022-11-07 | Howmedica Osteonics Corp. | Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is |
| 2021-03-22 | BIOPSYBELL S.R.L. | Products labeled as sterile were distributed, but may not have been sterilized. |
| 2021-03-22 | BIOPSYBELL S.R.L. | Products labeled as sterile were distributed, but may not have been sterilized. |
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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.