Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported April 4, 2018
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purchased to facilitate attachment and consolidation of patient equipment to one central patient care area. Devices commonly attached to IV poles include IV pumps, feeding pumps, and infusion fluid bags. Products used on: Giraffe OmniBed, Giraffe Warmers, Panda Warmers and Giraffe Incubators and Giraffe Shuttle. The IV pole also can be mounted to the Care Plus Incuba
There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander holding the patient or to the operator.
Ohmeda Medical recalled Rotating IV Pole Rotating IV Pole falls under the category classified as capital equ… - a moderate-severity action.
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equ… was recalled by Ohmeda Medical in April 4, 2018. Reason: There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander hold…. Check the official notice for the remedy. Verify recall #Z-1181-2018 with the FDA Devices before acting.
The recall
Ohmeda Medical issued this moderate-severity FDA Devices recall-There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander hold….
- Moderate
- severity level
- Class II
- classification
- April 4, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1181-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1181-2018) was formally reported on April 4, 2018, with the manufacturer initiating the action on December 1, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Ohmeda Medical is listed as the recalling firm, operating out of Laurel, MD. Federal records list the affected scope as 1,179 (1,004 US; 175 OUS).
The documented reason for this recall is: There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander holding the patient or to the operator. Distribution data in the federal record shows the product reached: USA (nationwide). 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, 3 from FDA Devices - 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 - 40,322 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
1,179 (1,004 US; 175 OUS)
Related Recalls
6
3 from same agency
Product description
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purchased to facilitate attachment and consolidation of patient equipment to one central patient care area. Devices commonly attached to IV poles include IV pumps, feeding pumps, and infusion fluid bags. Products used on: Giraffe OmniBed, Giraffe Warmers, Panda Warmers and Giraffe Incubators and Giraffe Shuttle. The IV pole also can be mounted to the Care Plus Incubator and Panda IWS.
Reason for recall
There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander holding the patient or to the operator.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1181-2018 |
| Date reported | April 4, 2018 |
| Date initiated | December 1, 2017 |
| Recalling firm | Ohmeda Medical |
| Firm location | Laurel, MD |
| Affected scope | 1,179 (1,004 US; 175 OUS) |
| Distribution | USA (nationwide) |
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-1181-2018) 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? ▼
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purchased to facilitate attachment and consolidation of patient equipment to one central patient care area. Devices commonly attached to IV poles include IV pumps, feeding pumps, and infusion fluid bags. Products used on: Giraffe OmniBed, Giraffe Warmers, Panda Warmers and Giraffe Incubators and Giraffe Shuttle. The IV pole also can be mounted to the Care Plus Incubator and Panda IWS.. Recalled by Ohmeda Medical. Units affected: 1,179 (1,004 US; 175 OUS).
Why was this product recalled? ▼
There is the potential for the Rotating IV Pole to fall. A fall could result in an injury to a bystander holding the patient or to the operator.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 4, 2018. Severity: Moderate. Recall number: Z-1181-2018.
Where was the recalled product distributed? ▼
Distribution: USA (nationwide).
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1181-2018) 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 April 4, 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.