Drug recall
Alabama DUI Kit (custom), Reorder No. ALDW1200, Manufactured by: Sirchie, 100 Hunter Place, Youngsville, NC…
FDA recall event 58394 · Class II · Sirchie Finger Print Labs Inc
Key facts
| Event ID | 58394 |
|---|---|
| Recall numbers | D-882-2011, D-883-2011, D-884-2011, D-885-2011, D-886-2011, D-887-2011, D-888-2011, D-889-2011, D-890-2011 |
| Recalling firm | Sirchie Finger Print Labs Inc |
| Product type | Drugs |
| Products | Alabama DUI Kit (custom), Reorder No. ALDW1200, Manufactured by: Sirchie, 100 Hunter Place, Youngsville, NC 27596, Alaska Blood Alcohol Kit (custom), Reorder No. AKBA100, Manufactured by: Sirchie, 100 Hunter Place, Youngsville, NC 27596, Blood Alcohol Kit, Reorder No. BSC100, BSK100, and BSK100CS-Case of 25, Manufactured by: Sirchie, 100 Hunter Place, Youngsville, NC 27596, Blood Alcohol/Urine Specimen Kit, Reorder No. BUK100, Manufactured by: Sirchie, 100 Hunter Place, Youngsville, NC 27596., Blood Specimen Collection Kit, Reorder No. BSC50 and BSC50CS-Case of 25, For Alcohol, Drug and Other Determinations, Manufactured by: Sirchie, 100 Hunter Place, Youngsville, NC 27596 and 4 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Microbial Contamination of Non-Sterile Products: This is a sub-recall of H&P, Povidine Iodine Prep Pads; The Kits under recall contain Povidine Prep Pads recalled by H&P Industries due to the…, Microbial Contamination of Non-Sterile Products: This is a sub-recall of H&P, Povidine Prep Pads; The Kits under recall contain Povidine Prep Pads recalled by H&P Industries due to the potential… |
| Initiation date | Apr 1, 2011 |
| Termination date | May 20, 2014 |
| City | Youngsville |
| State | NC |
| Country | United States |
| FEI number | 1000110931 |
At a glance
- 1–9 Products in this recall
- 1–9 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