CLASS I Device recall · Reported 12 Jun 2013 · FDA Enforcement Report
Part 510450 Disposable Infusion Pump recalled
Symbios Medical Products is recalling Part 510450 Disposable Infusion Pump, ...Elastomeric Pump(/hr ),... found in the, distributed nationwide in the US. The recall was initiated on 10 May 2013 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-1458-2013
- FDA event ID
- 65192
- Recalling firm
- Symbios Medical Products, Indianapolis, IN
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 10 May 2013
- FDA classified
- 6 Jun 2013
- Reported
- 12 Jun 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Infusion Pumps
Timeline
| 10 May 2013 | Recall initiated by company | |
| 6 Jun 2013 | Classified by FDA | +27 days |
| 12 Jun 2013 | 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
Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary recall of all GoPumps found in the GoPump Rapid Recovery System kits and all GoBlock kits manufactured with flow control components assembled prior to July 2012. The recall is being expanded after receiving additional reports relating to excessively high flow rates on the 150 mL reservoir, 2 mL/hr GOPump (PN510031), and the
Product as listed by the FDA
Part 510450 Disposable Infusion Pump, ...Elastomeric Pump 600 mL( 10mL/hr ),... found in the following kits GoBlock Kit 510458, Disposable Single Infusion Pump
Where it was distributed
US Nationwide distribution.
Questions about this recall
Is Part 510450 Disposable Infusion Pump, ...Elastomeric Pump(/hr ),... found in the recalled?
Yes. Symbios Medical Products recalled Part 510450 Disposable Infusion Pump, ...Elastomeric Pump(/hr ),... found in the on 10 May 2013. The recall is Class I and its status is Terminated. Recall number Z-1458-2013.
Why was it recalled?
Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary recall of all GoPumps found in the GoPump Rapid Recovery System kits and all GoBlock kits manufactured with flow control components assembled prior to July 2012. The recall is being expanded after receiving additional reports relating to excessively high flow rates on the 150 mL reservoir, 2 mL/hr GOPump (PN510031), and the
Which lots are affected?
Pump Part 510450, Lot 11-100351- Lot 12-101243 found in: GoBlock Kit 510458, Lot 11-100618 to 13-100703
Where was it sold?
US Nationwide distribution.
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Symbios Medical Products
All 12| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Part 510031 Disposable Single Infusion Pump recalled | Symbios Medical Products | Sterility | Nationwide |
| Device | CLASS I | Part 510613 Disposable Infusion Pump recalled | Symbios Medical Products | Other | Nationwide |
| Device | CLASS I | Part 510613 Disposable Infusion Pump recalled | Symbios Medical Products | Other | Nationwide |
| Device | CLASS I | Part 510121 Disposable Infusion Pump recalled | Symbios Medical Products | Sterility | Nationwide |
| Device | CLASS I | Part 510076 Disposable Dual Infusion Pump recalled | Symbios Medical Products | Sterility | Nationwide |
Other Infusion Pumps recalls
All 546| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Baxter Novum IQ Syringe Pump, Loaner recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter Novum IQ Syringe Pump recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS I | Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Plum Solo Precision IV Pump, v1.0.3 recalled by ICU Medical | ICU Medical | Other | Nationwide |
| Device | CLASS II | Intera Oncology Intera 3000 Hepatic Artery Infusion Pump recalled | Boston Scientific | Packaging Defects | Nationwide |