Johnson Matthey Cisplatin Active Pharmaceutical Ingredient Recall

Why it was recalled

cGMP Deviations: Potential glass contamination

Product description

Cisplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001

Lot numbers, UPCs & expiration codes

Lot #: B0101-161102, Exp. Dec 2021

Where it was sold

Nationwide within the United States

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-1881-2019
Classification: Class II
Status: Terminated
Recall initiated: Aug 29, 2019
FDA report date: Oct 2, 2019
Quantity: 26625 grams
Recall type: Voluntary: Firm initiated
Recalling firm: Johnson Matthey Inc.

Original FDA data

Every field from FDA enforcement report D-1881-2019, exactly as published.

Show all FDA fields

City: West Deptford
State: NJ
Status: Terminated
Country: United States
Event ID: 83457
Address: 2003 Nolte Dr
Code information: Lot #: B0101-161102, Exp. Dec 2021
Postal code: 08066-1727
Report date: Oct 2, 2019
Product type: Drugs
Recall number: D-1881-2019
Classification: Class II
Recalling firm: Johnson Matthey Inc.
Product quantity: 26625 grams
Termination date: Jan 21, 2022
Reason for recall: cGMP Deviations: Potential glass contamination
Voluntary / mandated: Voluntary: Firm initiated
Product description: Cisplatin Active Pharmaceutical Ingredient, Johnson Matthey Pharmaceutical Materials 2003 Nolte Drive, West Deptford, NJ 08066-1742 (856) 384-7001
Distribution pattern: Nationwide within the United States
Recall initiation date: Aug 29, 2019
Initial firm notification: Letter
Center classification date: Sep 25, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1881-2019, published Oct 2, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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.