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Class II: temporary or reversible health riskTerminated

Nephron Sterile Compounding Center 0.125% Bupivacaine HCl Injection Recall

0.125% Bupivacaine HCl Injection, USP, 62.5 mg/50 mL (1.25 mg/mL) syringes, packaged in…

Nephron Sterile Compounding Center LLC · West Columbia, SC

Risk level
Class II
Reported by FDA
Jul 27, 2022
Recall ID
D-1247-2022
Check your lot numberHow we source this data

Summary

Nephron Sterile Compounding Center recalled 0.125% Bupivacaine HCl Injection starting Jun 30, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1247-2022 on Jul 27, 2022. Reason: Lack of Assurance of Sterility. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility

Product description

0.125% Bupivacaine HCl Injection, USP, 62.5 mg/50 mL (1.25 mg/mL) syringes, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Ext., West Columbia, SC 29172, NDC: 69374-970-50

Lot numbers, UPCs & expiration codes

Lots: BH2001A, Exp. 7/15/2022; BH2002A, Exp. 8/7/2022; BH2004A, Exp. 8/22/2022; BH2005A, Exp. 9/2/2022; BH2006A, Exp. 9/14/2022; BH2007A, Exp. 9/29/2022; BH2008A, Exp. 10/3/2022; BH2010A, Exp. 10/19/2022

Where it was sold

Nationwide in the USA

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-1247-2022
Classification
Class II
Status
Terminated
Recall initiated
Jun 30, 2022
FDA report date
Jul 27, 2022
Quantity
6900 syringes
Recall type
Voluntary: Firm initiated
Recalling firm
Nephron Sterile Compounding Center LLC

Original FDA data

Every field from FDA enforcement report D-1247-2022, exactly as published.

Show all FDA fields
City
West Columbia
State
SC
Status
Terminated
Country
United States
Event ID
90512
Address
4500 12th Street Ext
Code information
Lots: BH2001A, Exp. 7/15/2022; BH2002A, Exp. 8/7/2022; BH2004A, Exp. 8/22/2022; BH2005A, Exp. 9/2/2022; BH2006A, Exp. 9/14/2022; BH2007A, Exp. 9/29/2022; BH2008A, Exp. 10/3/2022; BH2010A, Exp. 10/19/2022
Postal code
29172-3025
Report date
Jul 27, 2022
Product type
Drugs
Recall number
D-1247-2022
Classification
Class II
Recalling firm
Nephron Sterile Compounding Center LLC
Product quantity
6900 syringes
Termination date
Jun 17, 2024
Reason for recall
Lack of Assurance of Sterility
Voluntary / mandated
Voluntary: Firm initiated
Product description
0.125% Bupivacaine HCl Injection, USP, 62.5 mg/50 mL (1.25 mg/mL) syringes, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Ext., West Columbia, SC 29172, NDC: 69374-970-50
Distribution pattern
Nationwide in the USA
Recall initiation date
Jun 30, 2022
Initial firm notification
Letter
Center classification date
Jul 18, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1247-2022, published Jul 27, 2022. View the source record (openFDA) · FDA enforcement reports

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

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