Severity
Critical
CriticalClass ITerminated
FDA Devices recall · Reported March 12, 2014
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anest
There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from ano…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Mckesson Technologies INC. recalled McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a comp… - a critical-severity action.
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a comp… was recalled by Mckesson Technologies INC. in March 12, 2014. Reason: There was an occurrence where the patient case data did not match the patient data when the case was recalled…. Check the official notice for the remedy. Verify recall #Z-1060-2014 with the FDA Devices before acting.
The recall
Mckesson Technologies INC. issued this critical-severity FDA Devices recall-There was an occurrence where the patient case data did not match the patient data when the case was recalled….
- Critical
- severity level
- 10 units
- affected scope
- Class I
- classification
- March 12, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1060-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1060-2014) was formally reported on March 12, 2014, with the manufacturer initiating the action on March 15, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Mckesson Technologies INC. is listed as the recalling firm, operating out of Durham, NC. Federal records list the affected scope as 10.
The documented reason for this recall is: There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from another case. Distribution data in the federal record shows the product reached: Nationwide Distribution including CA, GA, IN, KY, MD, MI, OH, OK, and WA.. 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
10
Related Recalls
6
3 from same agency
Product description
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.
Reason for recall
There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from another case.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | Z-1060-2014 |
| Date reported | March 12, 2014 |
| Date initiated | March 15, 2013 |
| Recalling firm | Mckesson Technologies INC. |
| Firm location | Durham, NC |
| Affected scope | 10 |
| Distribution | Nationwide Distribution including CA, GA, IN, KY, MD, MI, OH, OK, and WA. |
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-1060-2014) 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.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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? ▼
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.. Recalled by Mckesson Technologies INC.. Units affected: 10.
Why was this product recalled? ▼
There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from another case.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 12, 2014. Severity: Critical. Recall number: Z-1060-2014.
Where was the recalled product distributed? ▼
Distribution: Nationwide Distribution including CA, GA, IN, KY, MD, MI, OH, OK, and WA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1060-2014) 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 March 12, 2014. 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.