CLASS II Device recall · Reported 17 Feb 2016 · FDA Enforcement Report
VS300 radiographic Cassette Holder or Wall Stand recalled by Del Medical
Del Medical is recalling VS300 radiographic Cassette Holder or Wall Stand, distributed nationwide in the US. The recall was initiated on 3 Dec 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-0762-2016
- FDA event ID
- 72798
- Recalling firm
- Del Medical, Bloomingdale, IL
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 3 Dec 2015
- FDA classified
- 5 Feb 2016
- Reported
- 17 Feb 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Imaging Equipment
Timeline
| 3 Dec 2015 | Recall initiated by company | |
| 5 Feb 2016 | Classified by FDA | +64 days |
| 17 Feb 2016 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The wall stand cassette holder can suddenly fall to the bottom of its travel, near the ground and contact patient.
Product as listed by the FDA
VS300 radiographic Cassette Holder or Wall Stand. For use in radiology department.
Where it was distributed
Worldwide Distribution-US (nationwide) and the countries of Canada, Costa Rica, Libya, Mexico, and Philippines.
Questions about this recall
Why was it recalled?
The wall stand cassette holder can suddenly fall to the bottom of its travel, near the ground and contact patient.
Which lots are affected?
Product # Serial # 110-5124G1 , 00019-0114 110-5124G1 , 00020-0114 110-5124G1 , 00092-0114 110-5124G1 , 00551-0314 110-5124G1 , 00512-0214 110-5124G1 , 00447-0214 110-5124G1 , 00016-0114 110-5124G1 , 00554-0314 110-5124G1 , 00094-0114 110-5124G1 , 00256-0214 110-5124G1 , 00741-0314 110-5124G1 , 00446-0214 110-5124G1 , 00017-0114 110-5124G1 , 00093-0114 110-5124G1 , 00236-0114 110-5124G1 , 00814-0414 110-5124G1 , 00815-0414 110-5124G1 , 00340-0214 110-5124G3 , 00995-0414 110-5124G1 , 00338-0214 110-5124G1 , 00552-0314 110-5124G1 , 00253-0214 110-5124G1 , 00445-0214 110-5124G1 , 00254-0214 110-5124G1 , 00095-0114 110-5124G1 , 00670-0314 110-5124G1 , 00252-0214 110-5124G1 , 00018-0114 110-5124G1 , 00669-0314 110-5124G1 , 00339-0214 110-5124G1 , 00444-0214 110-5124G1 , 00255-0214
Where was it sold?
Worldwide Distribution-US (nationwide) and the countries of Canada, Costa Rica, Libya, Mexico, and Philippines.
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 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.
Other products in this recall event
1 other product · FDA event 72798This product is part of a recall event; the main page for the event is VS200 radiographic Cassette Holder or Wall Stand recalled by Del Medical.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | VS200 radiographic Cassette Holder or Wall Stand recalled by Del Medical | Del Medical | Other | Nationwide |
More recalls from Del Medical
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | VS200 radiographic Cassette Holder or Wall Stand recalled by Del Medical | Del Medical | Other | Nationwide |
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| Device | CLASS II | Philips Azurion recalled by Philips Medical Systems | Philips Medical Systems Nederland B.v | Lead & Heavy Metals |