PlainRecalls
FDA Drug Moderate Class II Terminated

Heparin 10,000 U/Bupivacaine 0.5% 10 mL, Sodium Bicarbonate 8.4% 50 mL, 61 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

Reported: April 24, 2019 Initiated: April 2, 2019 #D-1158-2019

Product Description

Heparin 10,000 U/Bupivacaine 0.5% 10 mL, Sodium Bicarbonate 8.4% 50 mL, 61 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

Reason for Recall

Lack of sterility assurance.

Details

Units Affected
1 syringe
Distribution
Nationwide
Location
Bristol, TN

Frequently Asked Questions

What product was recalled?
Heparin 10,000 U/Bupivacaine 0.5% 10 mL, Sodium Bicarbonate 8.4% 50 mL, 61 mL Syringe, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.. Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy. Units affected: 1 syringe.
Why was this product recalled?
Lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 24, 2019. Severity: Moderate. Recall number: D-1158-2019.