PlainRecalls
FDA Drug Moderate Class II Terminated

Sn-DTPA Kit 10 mg, DTPA, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.

Reported: June 19, 2019 Initiated: May 28, 2019 #D-1404-2019

Product Description

Sn-DTPA Kit 10 mg, DTPA, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.

Reason for Recall

Lack of Processing Controls.

Details

Recalling Firm
Synthetopes Inc
Units Affected
82 vials
Distribution
Nationwide.
Location
Conway, SC

Frequently Asked Questions

What product was recalled?
Sn-DTPA Kit 10 mg, DTPA, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.. Recalled by Synthetopes Inc. Units affected: 82 vials.
Why was this product recalled?
Lack of Processing Controls.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 19, 2019. Severity: Moderate. Recall number: D-1404-2019.