Cordis a Johnson & Johnson Company, RadialSource Spring Wire Transradial Access Kit. Manufacturer...
FDA Device Recall #Z-1608-2013 — Class II — May 31, 2013
Recall Summary
| Recall Number | Z-1608-2013 |
| Classification | Class II — Moderate risk |
| Date Initiated | May 31, 2013 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Greatbatch Medical |
| Location | Minneapolis, MN |
| Product Type | Devices |
| Quantity | 550 kits (OUS) |
Product Description
Cordis a Johnson & Johnson Company, RadialSource Spring Wire Transradial Access Kit. Manufacturer Greatbatch Medical 2300 Berkshire Lane North, Minneapolis, MN 55441, Distributor Cordis Corporation 14201 North West 60th Avenue, Miami Lakes, Florida 33014. Baxter's lnfusors SV Elastomeric Infusion Device is a single-use, disposable elastomeric infusion pump indicated tor patients requiring slow, continuous intravenous, intra-arterial, subcutaneous, or epidural administration of medications at a constant flow rate. The device is also indicated for the administration of bolus doses of medication upon patient demand when used in conjunction with the Patient Control Module. lt is suitable for use in the hospital or home setting.
Reason for Recall
Cordis Corporation, Inc and Greatbatch Medical are recalling one lot of the cordis RADIALSOURCE Spring Wire Transradial Access Kit product. Some units were manufactured with an undersized vessel dilator tip, too small to slide over the guidewire.
Distribution Pattern
Worldwide Distribution - AUSTRIA, BELGIUM, SWITZERLAND, GERMANY, SPAIN, GREECE, HUNGARY, IRELAND, ISRAEL and ITALY.
Lot / Code Information
Manufacturing Lot : W18499722
Other Recalls from Greatbatch Medical
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-2055-2017 | Class II | Linear Straight Broach Handle (Rasp Handle) (Gr... | Apr 23, 2017 |
| Z-2782-2017 | Class II | Biosense Webster MobiCath Bi-Directional Guidin... | Feb 15, 2017 |
| Z-2781-2017 | Class II | ViaPeel PTFE Peelable Introducer 5FR, Part Numb... | Nov 11, 2016 |
| Z-1190-2017 | Class II | Offset Reamer Handle, T5766 Product Usage: ... | Oct 19, 2016 |
| Z-0623-2017 | Class II | Greatbatch Stiffer Coaxial Micro-Introducer. Mo... | Sep 8, 2016 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.