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Class II: temporary or reversible health riskTerminated

L. Perrigo Prednisone tablets Recall

Prednisone tablets, USP, 10mg, Rx Only, Units of Use

L. Perrigo Co. · Allegan, MI

Risk level
Class II
Reported by FDA
Jan 23, 2013
Recall ID
D-125-2013
Check your lot numberHow we source this data

Summary

L. Perrigo recalled Prednisone tablets starting Dec 17, 2012. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-125-2013 on Jan 23, 2013. Reason: Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward Pharmaceuticals. This is a sub-recall due to tablets contaminated with trace amounts of food-grade lubricant, as well as stainless steel inclusions. Status: Terminated.

Why it was recalled

Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward Pharmaceuticals. This is a sub-recall due to tablets contaminated with trace amounts of food-grade lubricant, as well as stainless steel inclusions

Product description

Prednisone tablets, USP, 10mg, Rx Only, Units of Use, NDC: a) 45802-303-67, 48-count Cartons, b) 45802-303-21, 21-count Cartons, Manufactured by: West-Ward Pharmaceutical Corporation, Eastown, NJ 07724, Distributed by: Perrigo, Allegan, MI 49040.

Lot numbers, UPCs & expiration codes

Lot #s: a) 2DV1238, Exp10/13; 2CV0623, 2CV0625, Exp 11/13; b) 2DV1239, Exp 10/13; 2CV0627, Exp 11/13

Where it was sold

Nationwide

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-125-2013
Classification
Class II
Status
Terminated
Recall initiated
Dec 17, 2012
FDA report date
Jan 23, 2013
Quantity
86,616 Tablets
Recall type
Voluntary: Firm initiated
Recalling firm
L. Perrigo Co.

Original FDA data

Every field from FDA enforcement report D-125-2013, exactly as published.

Show all FDA fields
City
Allegan
State
MI
Status
Terminated
Country
United States
Event ID
63966
Address
515 Eastern Ave
Code information
Lot #s: a) 2DV1238, Exp10/13; 2CV0623, 2CV0625, Exp 11/13; b) 2DV1239, Exp 10/13; 2CV0627, Exp 11/13
Postal code
49010-9070
Report date
Jan 23, 2013
Product type
Drugs
Recall number
D-125-2013
Classification
Class II
Recalling firm
L. Perrigo Co.
Product quantity
86,616 Tablets
Termination date
Jan 6, 2014
Reason for recall
Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward Pharmaceuticals. This is a sub-recall due to tablets contaminated with trace amounts of food-grade lubricant, as well as stainless steel inclusions
Voluntary / mandated
Voluntary: Firm initiated
Product description
Prednisone tablets, USP, 10mg, Rx Only, Units of Use, NDC: a) 45802-303-67, 48-count Cartons, b) 45802-303-21, 21-count Cartons, Manufactured by: West-Ward Pharmaceutical Corporation, Eastown, NJ 07724, Distributed by: Perrigo, Allegan, MI 49040.
Distribution pattern
Nationwide
Recall initiation date
Dec 17, 2012
Initial firm notification
Letter
Center classification date
Jan 14, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-125-2013, published Jan 23, 2013. View the source record (openFDA) · FDA enforcement reports

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

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