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Class II: temporary or reversible health riskTerminated

SCA Pharmaceuticals Heparin Sodium 5 Recall

Heparin Sodium 5,000 units in 0

SCA Pharmaceuticals · Windsor, CT

Risk level
Class II
Reported by FDA
Aug 19, 2020
Recall ID
D-1495-2020
Check your lot numberHow we source this data

Summary

SCA Pharmaceuticals recalled Heparin Sodium 5 starting Jul 29, 2020. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1495-2020 on Aug 19, 2020. Reason: Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint. Status: Terminated.

Why it was recalled

Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint.

Product description

Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx only, SCA Pharmaceuticals 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0650-46

Lot numbers, UPCs & expiration codes

Lot #: 1220018755, Exp. Date 7/30/2020; 1220018861, 1220018850, Exp. Date 8/4/2020; 1220018899, Exp. Date 8/5/2020; 1220019027, Exp. Date 8/11/2020; 1220019075, Exp. Date 8/12/2020; 1220019243, Exp. Date 8/20/2020; 1220019439, 1220019279, 1220019392, Exp. Date 8/24/2020; 1220019488, Exp. Date 8/26/2020

Where it was sold

Product was distributed 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-1495-2020
Classification
Class II
Status
Terminated
Recall initiated
Jul 29, 2020
FDA report date
Aug 19, 2020
Quantity
3,932 bags
Recall type
Voluntary: Firm initiated
Recalling firm
SCA Pharmaceuticals

Original FDA data

Every field from FDA enforcement report D-1495-2020, exactly as published.

Show all FDA fields
City
Windsor
State
CT
Status
Terminated
Country
United States
Event ID
86194
Address
755 Rainbow Rd Ste B
Code information
Lot #: 1220018755, Exp. Date 7/30/2020; 1220018861, 1220018850, Exp. Date 8/4/2020; 1220018899, Exp. Date 8/5/2020; 1220019027, Exp. Date 8/11/2020; 1220019075, Exp. Date 8/12/2020; 1220019243, Exp. Date 8/20/2020; 1220019439, 1220019279, 1220019392, Exp. Date 8/24/2020; 1220019488, Exp. Date 8/26/2020
Postal code
06095-1024
Report date
Aug 19, 2020
Product type
Drugs
Recall number
D-1495-2020
Classification
Class II
Recalling firm
SCA Pharmaceuticals
Product quantity
3,932 bags
Termination date
Mar 17, 2021
Reason for recall
Subpotent Drug: Out-of-Specification potency results at the 30-day stability timepoint.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL bag (5 units/mL), Rx only, SCA Pharmaceuticals 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0650-46
Distribution pattern
Product was distributed nationwide within the United States.
Recall initiation date
Jul 29, 2020
Initial firm notification
Letter
Center classification date
Aug 12, 2020

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1495-2020, published Aug 19, 2020. View the source record (openFDA) · FDA enforcement reports

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

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