CLASS II Device recall · Reported 16 Apr 2014 · FDA Enforcement Report
Drain Kit Full Fluted with Trocar and S-Vac Bulb recalled
Aspen Surgical Products is recalling Drain Kit Full Fluted with Trocar and S-Vac Bulb, Sterile Intended for closed wound, distributed in 35 states. The recall was initiated on 20 Mar 2014 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1426-2014
- FDA event ID
- 67757
- Recalling firm
- Aspen Surgical Products, Caledonia, MI
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 20 Mar 2014
- FDA classified
- 7 Apr 2014
- Reported
- 16 Apr 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Sterility
- Device type
- Surgical Instruments
Timeline
| 20 Mar 2014 | Recall initiated by company | |
| 7 Apr 2014 | Classified by FDA | +18 days |
| 16 Apr 2014 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
19FR Drain Kit Full Fluted with Trocar and 100ml S-Vac Bulb, Sterile (10/case) Intended for closed wound suction drainage
Where it was distributed
Worldwide Distribution - USA including LA, MA, NH, TX, FL, OH, NC, PA, CA, UT, TN, MI, CO, WY, OK, WA, MN, PA, IN, VA, IA, IL, MD, CT, DE, SC, NY, AR, MA, AZ, NJ, MO, GA, KS, WV, NE, NC, Puerto Rico, and Internationally to Canada, UAE, England, Italy, Belgium, Costa Rica, and Ecuador.
ArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIowaIllinoisIndianaKansasLouisianaMassachusettsMarylandMichiganMinnesotaMissouriNorth CarolinaNebraska
Questions about this recall
Why was it recalled?
The recall has been initiated due to a potential compromise of the sterile barrier of the Surgidyne Wound Drainage and Surgidyne Bulb Evacuator & Collection System medical devices.
Which lots are affected?
Product Number 332265
Where was it sold?
Worldwide Distribution - USA including LA, MA, NH, TX, FL, OH, NC, PA, CA, UT, TN, MI, CO, WY, OK, WA, MN, PA, IN, VA, IA, IL, MD, CT, DE, SC, NY, AR, MA, AZ, NJ, MO, GA, KS, WV, NE, NC, Puerto Rico, and Internationally to Canada, UAE, England, Italy, Belgium, Costa Rica, and Ecuador.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
18 other products · FDA event 67757This product is part of a recall event; the main page for the event is Drain Kit Full Fluted with Trocar and S-Vac Bulb recalled.
More recalls from Aspen Surgical Products
All 23| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Marco Shoulder Stabilization Kit, Product recalled | Aspen Surgical Products | Sterility | Nationwide |
| Device | CLASS II | Jessie Sterile Arm Suspension Kit, Product recalled | Aspen Surgical Products | Sterility | Nationwide |
| Device | CLASS II | Norton Arm Kit, Product recalled by Aspen Surgical Products | Aspen Surgical Products | Sterility | Nationwide |
| Device | CLASS II | Drain Kit Flat Full Perforated with Trocar, Saber Bulb recalled | Aspen Surgical Products | Sterility | 35 states |
| Device | CLASS II | Drain Kit Flat Full Perforated with Trocar recalled | Aspen Surgical Products | Sterility | 35 states |
Other Surgical Instruments recalls
All 3,809| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Medline Convenience Kits: IV Start KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled | ConMed | Other | Nationwide |