Food, drugs, devices › Pride Mobility Products Corp
Device recall: Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.
FDA enforcement event 57350 is a device recall by Pride Mobility Products Corp of Exeter, PA, initiated 26 Nov 2010 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 89% of the 37 device enforcement events initiated in 2010 carry the same class.
Status: Terminated, terminated 22 Mar 2013. Initiation: voluntary: firm initiated. Pride Mobility Products Corp has 3 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Pride Mobility Products Corp, Exeter, PA.
Reason for recall
"The main harness connector was manufactured without the required back shield sealing protection. As a result, there is the potential for water to seep through the nonconforming harness."
Distribution
"Worldwide Distribution"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1941-2012 | Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat. | 186 | Class II | Terminated | 11 Jul 2012 |
Context
Other enforcement events for Pride Mobility Products Corp
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 25 Jun 2026 | Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version: 2.0.11 | Device | Class II | 13 |
| 1 Dec 2016 | TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device | Device | Class II | 1 |
All 3 events for Pride Mobility Products Corp
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "The main harness connector was manufactured without the required back shield sealing protection. As a result, there is the potential for water to seep through the nonconforming harness."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Worldwide Distribution"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 22 Mar 2013. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.