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Access HLT Plus Exam Table
The Brewer Company LLC · Model 6800PLUS · UDI-DI 07285641068005
10
510(k) clearances
80
Adverse events
15
Recalls
48
Facilities
Description
These tables are designed to provide positioning and support of patients during general examinations and minor procedures conducted by qualified medical professionals.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-05 | Oakworks Inc | Backrest platform stress fracture - the table is not operational in an inclined position |
| 2023-12-05 | Oakworks Inc | Backrest platform stress fracture - the table is not operational in an inclined position |
| 2023-12-05 | Oakworks Inc | Backrest platform stress fracture - the table is not operational in an inclined position |
| 2023-12-05 | Oakworks Inc | Backrest platform stress fracture - the table is not operational in an inclined position |
| 2021-06-29 | Oakworks Inc | Weld failure- the bracket attaches the tabletop tilting actuator to the tabletop frame. If the bracket weld fails, the tabletop tilting action is non-functional |
| 2019-05-06 | Maquet Cardiovascular Us Sales, Llc | User may suffer an electric shock when coming in contact with the exposed electronic components |
| 2018-03-29 | Brewer Company, LLC | One lot, the wire harness was over-crimped on some of the connectors that go to the two vertical side switches on the exam table. |
| 2016-09-02 | Heritage Medical Products, Inc. | Potential for bed to drop suddenly at the head while a patient is laying on it. |
| 2014-07-10 | Medical Positioning Inc | Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a c |
| 2014-07-10 | Medical Positioning Inc | Excessive weight on the table will cause tables with the affected component to drop into the Trendelenburg position more rapidly than normal. The product was manufactured with a c |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.