Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported September 26, 2018
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Med-Mizer, Inc. recalled PR1000 Pivot Rehab Bed AC powered adjustable bed. - a moderate-severity action.
PR1000 Pivot Rehab Bed AC powered adjustable bed. was recalled by Med-Mizer, Inc. in September 26, 2018. Reason: Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables ma…. Check the official notice for the remedy. Verify recall #Z-3183-2018 with the FDA Devices before acting.
The recall
Med-Mizer, Inc. issued this moderate-severity FDA Devices recall-Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables ma….
- Moderate
- severity level
- 230 units
- affected scope
- Class II
- classification
- September 26, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-3183-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-3183-2018) was formally reported on September 26, 2018, with the manufacturer initiating the action on July 25, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Med-Mizer, Inc. is listed as the recalling firm, operating out of Batesville, IN. Federal records list the affected scope as 230 units.
The documented reason for this recall is: Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until… Distribution data in the federal record shows the product reached: The products were distributed to the following US states: AR, AZ, FL, GA, IA, ID, IL, IN, KY, ME, MI, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, and WI. The products were distributed to the foll…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
230 units
Related Recalls
6
0 from same agency
Product description
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Reason for recall
Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-3183-2018 |
| Date reported | September 26, 2018 |
| Date initiated | July 25, 2018 |
| Recalling firm | Med-Mizer, Inc. |
| Firm location | Batesville, IN |
| Affected scope | 230 units |
| Distribution | The products were distributed to the following US states: AR, AZ, FL, GA, IA, ID, IL, IN, KY, ME, MI, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, and WI. The products were distributed to the following foreign countr… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-3183-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
PR1000 Pivot Rehab Bed AC powered adjustable bed.. Recalled by Med-Mizer, Inc.. Units affected: 230 units.
Why was this product recalled? ▼
Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 26, 2018. Severity: Moderate. Recall number: Z-3183-2018.
Where was the recalled product distributed? ▼
Distribution: The products were distributed to the following US states: AR, AZ, FL, GA, IA, ID, IL, IN, KY, ME, MI, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, and WI. The products were distributed to the following foreign countries: Canada, China, and Denmark..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-3183-2018) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported September 26, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.