FindMyRecallSubscribe
Class III: unlikely to cause harmTerminated

Pharmedium Services Ropivacaine HCl 0 Recall

Ropivacaine HCl 0

Pharmedium Services Llc · Lake Forest, IL

Risk level
Class III
Reported by FDA
Jul 12, 2017
Recall ID
D-0932-2017
Check your lot numberHow we source this data

Summary

Pharmedium Services recalled Ropivacaine HCl 0 starting Feb 15, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0932-2017 on Jul 12, 2017. Reason: Labeling: Incorrect or Missing Lot and/or Exp Date. Status: Terminated.

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Exp Date

Product description

Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25

Lot numbers, UPCs & expiration codes

Lot: 170270192s Lot: 170330167s Lot: 170320087s Ex.: 01/01/1900

Where it was sold

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-0932-2017
Classification
Class III
Status
Terminated
Recall initiated
Feb 15, 2017
FDA report date
Jul 12, 2017
Quantity
147 I.V. pumps
Recall type
Voluntary: Firm initiated
Recalling firm
Pharmedium Services Llc

Original FDA data

Every field from FDA enforcement report D-0932-2017, exactly as published.

Show all FDA fields
City
Lake Forest
State
IL
Status
Terminated
Country
United States
Event ID
77374
Address
150 N Field Dr
Code information
Lot: 170270192s Lot: 170330167s Lot: 170320087s Ex.: 01/01/1900
Postal code
60045-4847
Report date
Jul 12, 2017
Product type
Drugs
Recall number
D-0932-2017
Classification
Class III
Recalling firm
Pharmedium Services Llc
Product quantity
147 I.V. pumps
Termination date
Jan 13, 2020
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date
Voluntary / mandated
Voluntary: Firm initiated
Product description
Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
Distribution pattern
Nationwide
Recall initiation date
Feb 15, 2017
Initial firm notification
Telephone
Center classification date
Jul 2, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0932-2017, published Jul 12, 2017. 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.

How we source and update recall data · Report incorrect information

Other recent drug recalls