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Class II: temporary or reversible health riskTerminated

JD & SN Inc., dba Moses Lake Professional Pharmacy Chorionic Gonadotropin Recall

CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0

JD & SN Inc., dba Moses Lake Professional Pharmacy · Moses Lake, WA

Risk level
Class II
Reported by FDA
Nov 4, 2015
Recall ID
D-0064-2016
Check your lot numberHow we source this data

Summary

JD & SN Inc., dba Moses Lake Professional Pharmacy recalled Chorionic Gonadotropin starting Jul 24, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0064-2016 on Nov 4, 2015. Reason: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

Product description

CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0.1 ML, vial sizes: 4 mL; 5 mL; 6 mL; 7.5 mL ; 9 mL, 10 mL; 12 mL; 15 mL; 20 mL; 28 mL; Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Lot numbers, UPCs & expiration codes

11032014@10, 12082014@3, t01082015@26, t03092015@26, t03132015@13, t03162015@12, t03242015@19, t04092015@21, t05132015@28, t05132015@44, t05202015@22, t05262015@14, t05272015@36, t06172015@27, t06182015@7, t06242015@9, t06292015@11, t07092015@42, t07102015@25, t08012014@1, t09122014@19, t09252014@4, t12242014@2, and t12312014@8.

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-0064-2016
Classification
Class II
Status
Terminated
Recall initiated
Jul 24, 2015
FDA report date
Nov 4, 2015
Quantity
9 (4mL), 4 (5mL) vials, 9 (6mL) vials, 5 (7.5mL) vials, 4 (10mL) vials, 5 (9mL) vials, 3 (12mL) vials, 2 (15mL) vials, 1 (20mL), 1 (28mL) vials
Recall type
Voluntary: Firm initiated
Recalling firm
JD & SN Inc., dba Moses Lake Professional Pharmacy

Original FDA data

Every field from FDA enforcement report D-0064-2016, exactly as published.

Show all FDA fields
City
Moses Lake
State
WA
Status
Terminated
Country
United States
Event ID
71806
Address
1555 Pilgrim St
Code information
11032014@10, 12082014@3, t01082015@26, t03092015@26, t03132015@13, t03162015@12, t03242015@19, t04092015@21, t05132015@28, t05132015@44, t05202015@22, t05262015@14, t05272015@36, t06172015@27, t06182015@7, t06242015@9, t06292015@11, t07092015@42, t07102015@25, t08012014@1, t09122014@19, t09252014@4, t12242014@2, and t12312014@8.
Postal code
98837-4623
Report date
Nov 4, 2015
Product type
Drugs
Recall number
D-0064-2016
Classification
Class II
Recalling firm
JD & SN Inc., dba Moses Lake Professional Pharmacy
Product quantity
9 (4mL), 4 (5mL) vials, 9 (6mL) vials, 5 (7.5mL) vials, 4 (10mL) vials, 5 (9mL) vials, 3 (12mL) vials, 2 (15mL) vials, 1 (20mL), 1 (28mL) vials
Termination date
Apr 13, 2016
Reason for recall
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Voluntary / mandated
Voluntary: Firm initiated
Product description
CHORIONIC GONADOTROPIN, Injectable Solution, 200 UNITS/0.1 ML, vial sizes: 4 mL; 5 mL; 6 mL; 7.5 mL ; 9 mL, 10 mL; 12 mL; 15 mL; 20 mL; 28 mL; Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Distribution pattern
Nationwide
Recall initiation date
Jul 24, 2015
Initial firm notification
Press Release
Center classification date
Oct 27, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0064-2016, published Nov 4, 2015. 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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