CLASS I Device recall · Reported 16 Mar 2016 · FDA Enforcement Report
RediGuard IAB: 30cc recalled by Arrow International, Inc.
Arrow International, Inc., Division of Teleflex Medical is recalling RediGuard IAB: 30cc, distributed nationwide in the US. The recall was initiated on 10 Feb 2016 and the FDA has classified it as Class I.
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-1061-2016
- FDA event ID
- 73266
- Recalling firm
- Arrow International, Inc., Division of Teleflex Medical, Everett, MA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 10 Feb 2016
- FDA classified
- 10 Mar 2016
- Reported
- 16 Mar 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Heart & Vascular Devices
Timeline
| 10 Feb 2016 | Recall initiated by company | |
| 10 Mar 2016 | Classified by FDA | +29 days |
| 16 Mar 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
Product as listed by the FDA
RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic balloon counterpulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle.
Where it was distributed
Worldwide Distribution: US (Nationwide) and countries of: Argentina, Australia, Belgium, Brunei Darussalam, Brazil, Bahamas, Canada, Chile, China, Colombia, Ecuador, Guatemala, Hong Kong, Indonesia, India, Japan, Korea (Republic of [South] Korea), Myanmar, Mexico, Malaysia, Nepal, New Zealand, Panama, Peru, Philippines, Pakistan, Singapore, Thailand, Trinidad and Tobago, Taiwan, Uruguay, Viet Nam, and South Africa (Zuid Afrika).
Questions about this recall
Why was it recalled?
The sheath body may become separated from the sheath hub. If the separation occurs, there is a potential for bleeding from the device.
Which lots are affected?
Batch:18F14A0041 18F14C0003 18F14C0006 18F14C0021 18F14C0026 18F14C0027 18F14C0028 18F14E0039 18F14E0055 18F14E0058 18F14F0035 18F14F0038 18F14F0054 18F14G0057 18F14G0077 18F14H0011 18F15B0023 18F15C0001 18F15C0008 18F15C0026 18F15D0028 18F15F0027 18F15F0037 18F15G0003 18F15G0011 18F15G0032 18F15H0046 18F15M0009
Where was it sold?
Worldwide Distribution: US (Nationwide) and countries of: Argentina, Australia, Belgium, Brunei Darussalam, Brazil, Bahamas, Canada, Chile, China, Colombia, Ecuador, Guatemala, Hong Kong, Indonesia, India, Japan, Korea (Republic of [South] Korea), Myanmar, Mexico, Malaysia, Nepal, New Zealand, Panama, Peru, Philippines, Pakistan, Singapore, Thailand, Trinidad and Tobago, Taiwan, Uruguay, Viet Nam, and South Africa (Zuid Afrika).
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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
8 other products · FDA event 73266This product is part of a recall event; the main page for the event is Percutaneous Insertion Tray recalled by Arrow International, Inc..
More recalls from Arrow International, Inc., Division of Teleflex Medical
All 9| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | FiberOptix Ultra 8 IAB: 40cc recalled by Arrow International, Inc. | Arrow International, Inc., Division of Teleflex Medical | Other | Nationwide |
| Device | CLASS I | Percutaneous Insertion Tray recalled by Arrow International, Inc. | Arrow International, Inc., Division of Teleflex Medical | Other | Nationwide |
| Device | CLASS I | UltraFlex IAB recalled by Arrow International, Inc. | Arrow International, Inc., Division of Teleflex Medical | Other | Nationwide |
| Device | CLASS I | FiberOptix Ultra 8 IAB: 30cc The Arrow¿ IAB is utilized recalled | Arrow International, Inc., Division of Teleflex Medical | Other | Nationwide |
| Device | CLASS I | UltraFlex IAB recalled by Arrow International, Inc. | Arrow International, Inc., Division of Teleflex Medical | Other | Nationwide |
Other Heart & Vascular Devices recalls
All 6,199| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Getinge PVC Thoracic Catheter, Soft PVC Right Angle recalled | Atrium Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes: *Bardex¿ I.C recalled | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Getinge PVC Thoracic Catheter, Firm PVC Straight recalled | Atrium Medical | Potency & Assay | Nationwide |