Drug recall
Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code: E258328 The Valleylab Laparoscopic…
FDA recall event 74602 · Class II · Medtronic
Key facts
| Event ID | 74602 |
|---|---|
| Recall numbers | Z-2554-2016, Z-2555-2016, Z-2556-2016, Z-2557-2016, Z-2558-2016, Z-2559-2016, Z-2560-2016, Z-2561-2016, Z-2562-2016, Z-2563-2016, Z-2564-2016, Z-2565-2016 and 13 more |
| Recalling firm | Medtronic |
| Product type | Devices |
| Products | Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code: E258328 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical…, Valleylab Laparoscopic Argon Modified Flat l Electrode 28CM Item Code: E258128 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical…, Valleylab Laparoscopic Argon Sharp Needle Electrode 28CM Item Code: E258228 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical…, Valleylab Laparoscopic Curved Spatula Electrode 28CM Item Code: E278128 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures…, Valleylab Laparoscopic Curved Spatula Electrode 36CM Item Code: E277136 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures… and 20 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for compromise of the package resulting in a breach of the sterile barrier |
| Initiation date | Jul 8, 2016 |
| Report date | Aug 24, 2016 |
| Termination date | Aug 8, 2018 |
| City | North Haven |
| State | CT |
| Country | United States |
| FEI number | 3011795455 |
At a glance
- 10–99 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: