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Class II: temporary or reversible health riskTerminated

Medical Supply Liquidators L-Carnitine Injection 100 mg/ml Recall

L-Carnitine Injection USP 100 mg/ml, packaged in 30 ml vials, Sterile, For IM or Deep S…

Medical Supply Liquidators Llc · Clive, IA

Risk level
Class II
Reported by FDA
Aug 13, 2014
Recall ID
D-1532-2014
Check your lot numberHow we source this data

Summary

Medical Supply Liquidators recalled L-Carnitine Injection 100 mg/ml starting Jun 25, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1532-2014 on Aug 13, 2014. Reason: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufacturing firm is not registered with the FDA as a drug manufacturer. Status: Terminated.

Why it was recalled

Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufacturing firm is not registered with the FDA as a drug manufacturer

Product description

L-Carnitine Injection USP 100 mg/ml, packaged in 30 ml vials, Sterile, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.

Lot numbers, UPCs & expiration codes

All lot numbers and exp dates

Where it was sold

Nationwide and Foriegn distribution was made to Canada, United Kingdom, Australia, Slovenia, Germany, Spain, Finland and Croatia.

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-1532-2014
Classification
Class II
Status
Terminated
Recall initiated
Jun 25, 2014
FDA report date
Aug 13, 2014
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Medical Supply Liquidators Llc

Original FDA data

Every field from FDA enforcement report D-1532-2014, exactly as published.

Show all FDA fields
City
Clive
State
IA
Status
Terminated
Country
United States
Event ID
68626
Address
10500 Hickman Rd Ste F
Code information
All lot numbers and exp dates
Postal code
50325-3706
Report date
Aug 13, 2014
Product type
Drugs
Recall number
D-1532-2014
Classification
Class II
Recalling firm
Medical Supply Liquidators Llc
Termination date
Mar 14, 2017
Reason for recall
Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufacturing firm is not registered with the FDA as a drug manufacturer
Voluntary / mandated
Voluntary: Firm initiated
Product description
L-Carnitine Injection USP 100 mg/ml, packaged in 30 ml vials, Sterile, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
Distribution pattern
Nationwide and Foriegn distribution was made to Canada, United Kingdom, Australia, Slovenia, Germany, Spain, Finland and Croatia.
Recall initiation date
Jun 25, 2014
Initial firm notification
E-Mail
Center classification date
Aug 6, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1532-2014, published Aug 13, 2014. 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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