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Class II: temporary or reversible health riskTerminated

Mckesson Medical-Surgical Inc. Corporate Office Epidural Tray Recall

Epidural Tray, Nerve Block Single shot, Rx only, # 182207, MFG: Avanos Medical Sales LLC

Mckesson Medical-Surgical Inc. Corporate Office · Richmond, VA

Risk level
Class II
Reported by FDA
Jun 15, 2022
Recall ID
D-1010-2022
Check your lot numberHow we source this data

Summary

Mckesson Medical-Surgical Inc. Corporate Office recalled Epidural Tray starting Apr 13, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1010-2022 on Jun 15, 2022. Reason: cGMP deviations: Temperature abuse. Status: Terminated.

Why it was recalled

cGMP deviations: Temperature abuse

Product description

Epidural Tray, Nerve Block Single shot, Rx only, # 182207, MFG: Avanos Medical Sales LLC

Lot numbers, UPCs & expiration codes

McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.

Where it was sold

USA nationwide.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1010-2022
Classification
Class II
Status
Terminated
Recall initiated
Apr 13, 2022
FDA report date
Jun 15, 2022
Quantity
1 case
Recall type
Voluntary: Firm initiated
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office

Original FDA data

Every field from FDA enforcement report D-1010-2022, exactly as published.

Show all FDA fields
City
Richmond
State
VA
Status
Terminated
Country
United States
Event ID
89646
Address
9954 Maryland Drive
Address (line 2)
Deep Run Iii Ste. 4000
Code information
McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Postal code
23233
Report date
Jun 15, 2022
Product type
Drugs
Recall number
D-1010-2022
Classification
Class II
Recalling firm
Mckesson Medical-Surgical Inc. Corporate Office
Product quantity
1 case
Termination date
Nov 30, 2023
Reason for recall
cGMP deviations: Temperature abuse
Voluntary / mandated
Voluntary: Firm initiated
Product description
Epidural Tray, Nerve Block Single shot, Rx only, # 182207, MFG: Avanos Medical Sales LLC
Distribution pattern
USA nationwide.
Recall initiation date
Apr 13, 2022
Initial firm notification
Letter
Center classification date
Jun 9, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1010-2022, published Jun 15, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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