CLASS II Device recall · Reported 15 Jul 2015 · FDA Enforcement Report
Arthroscopy Pack - contains Devon Light Glove Used during surgery recalled
Stradis Healthcare is recalling Arthroscopy Pack - contains Devon Light Glove Used during surgery, distributed nationwide in the US. The recall was initiated on 20 Apr 2015 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-2041-2015
- FDA event ID
- 71130
- Recalling firm
- Stradis Healthcare, Lawrenceville, GA
- Classification
- Class II
- Status
- Completed
- Recall initiated
- 20 Apr 2015
- FDA classified
- 7 Jul 2015
- Reported
- 15 Jul 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Surgical Instruments
Timeline
| 20 Apr 2015 | Recall initiated by company | |
| 7 Jul 2015 | Classified by FDA | +78 days |
| 15 Jul 2015 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Product as listed by the FDA
Arthroscopy Pack - contains Devon Light Glove Used during surgery
Where it was distributed
Distribution US nationwide to AL, AK, CA, DE, FL, GA, HI, ID, IL, IN, KS, KY, ME, MD, MA, MI, MS, MO, NM, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA; Canada and Dubai
Nationwide AlaskaAlabamaCaliforniaDelawareFloridaGeorgiaHawaiiIdahoIllinoisIndianaKansasKentuckyMassachusettsMarylandMaineMichiganMissouriMississippiNorth CarolinaNew Jersey
Questions about this recall
Why was it recalled?
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Which lots are affected?
Pack 888-2605
Where was it sold?
Distribution US nationwide to AL, AK, CA, DE, FL, GA, HI, ID, IL, IN, KS, KY, ME, MD, MA, MI, MS, MO, NM, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA; Canada and Dubai
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
50 other products · FDA event 71130This product is part of a recall event; the main page for the event is Lima Pack - contains Devon Light Glove Used during surgery recalled.
More recalls from Stradis Healthcare
All 71| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Hct Central Line Insertion Tray, I recalled by Stradis Healthcare | Stradis Healthcare | Sterility | Nationwide |
| Device | CLASS II | HCT, 2 Port, Sterile, Triple Packaged, 10 EVA BAGS/Pack recalled | Stradis Healthcare | Sterility | Nationwide |
| Device | CLASS II | Tacy Medical, Inc Port Access Tray, Sterile, Qty recalled | Stradis Healthcare | Sterility | Nationwide |
| Device | CLASS II | Picc Kit, 10/cs, Access Medical Label recalled by Stradis Healthcare | Stradis Healthcare | Sterility | Nationwide |
| Device | CLASS II | Henry Shein Cysto Set UP Pack recalled by Stradis Healthcare | Stradis Healthcare | Sterility | Nationwide |
Other Surgical Instruments recalls
All 3,816| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | REF:2B5LT Ethicon Endo-Surgery recalled by Stryker Sustainability | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | REF:B11LT Ethicon Endo-Surgery, Inc. Xcel Bladeless Trocar recalled | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | REF:B12LT Ethicon Endo-Surgery, Inc. Xcel Bladeless Trocar recalled | Stryker Sustainability Solutions | Device Malfunction | Nationwide |
| Device | CLASS II | Hemospray Endoscopic Hemostat recalled by Wilson-Cook Medical | Wilson-Cook Medical | Device Malfunction | Nationwide |
| Device | CLASS II | REF:B5LT Ethicon Endo-Surgery recalled by Stryker Sustainability | Stryker Sustainability Solutions | Device Malfunction | Nationwide |