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Class II: temporary or reversible health riskTerminated

Perry Drug Tri Mix PF SYR 0 Recall

Tri Mix PF SYR 0

Perry Drug Inc. · Overland Park, KS

Risk level
Class II
Reported by FDA
Dec 3, 2014
Recall ID
D-0273-2015
Check your lot numberHow we source this data

Summary

Perry Drug recalled Tri Mix PF SYR 0 starting Nov 7, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0273-2015 on Dec 3, 2014. Reason: Lack of sterility assurance;All lots of sterile products compounded by the pharmacy that are within expiry were recalled due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection. Status: Terminated.

Why it was recalled

Lack of sterility assurance;All lots of sterile products compounded by the pharmacy that are within expiry were recalled due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

Product description

Tri Mix PF SYR 0.5 mL Inj., Compounded Rx, 10 each, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-5036-49

Lot numbers, UPCs & expiration codes

141021FF, 11/21/14; 141028CC, 11/28/14

Where it was sold

Kansas and Missouri

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-0273-2015
Classification
Class II
Status
Terminated
Recall initiated
Nov 7, 2014
FDA report date
Dec 3, 2014
Quantity
20 prefilled syringes
Recall type
Voluntary: Firm initiated
Recalling firm
Perry Drug Inc.

Original FDA data

Every field from FDA enforcement report D-0273-2015, exactly as published.

Show all FDA fields
City
Overland Park
State
KS
Status
Terminated
Country
United States
Event ID
69674
Address
12200 W 106th St Ste 140
Code information
141021FF, 11/21/14; 141028CC, 11/28/14
Postal code
66215-2305
Report date
Dec 3, 2014
Product type
Drugs
Recall number
D-0273-2015
Classification
Class II
Recalling firm
Perry Drug Inc.
Product quantity
20 prefilled syringes
Termination date
Nov 3, 2015
Reason for recall
Lack of sterility assurance;All lots of sterile products compounded by the pharmacy that are within expiry were recalled due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Tri Mix PF SYR 0.5 mL Inj., Compounded Rx, 10 each, Compounded Rx, Perry Drug Compounding Pharmacy, Overland Park, KS --- NDC 88888-5036-49
Distribution pattern
Kansas and Missouri
Recall initiation date
Nov 7, 2014
Initial firm notification
Letter
Center classification date
Nov 24, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0273-2015, published Dec 3, 2014. View the source record (openFDA) · FDA enforcement reports

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

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