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Class II: temporary or reversible health riskTerminated

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

METHYLCOBALAMIN, Injectable Solution, 15 MG/ML, syringe sizes: 5 mL

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

Risk level
Class II
Reported by FDA
Nov 4, 2015
Recall ID
D-0104-2016
Check your lot numberHow we source this data

Summary

JD & SN Inc., dba Moses Lake Professional Pharmacy recalled Methylcobalamin starting Jul 24, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0104-2016 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

METHYLCOBALAMIN, Injectable Solution, 15 MG/ML, syringe sizes: 5 mL; 6 mL; 10 mL; 15 mL; 20 mL; 30 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

t12312014@6, t12042014@26, t11252014@31, t10302014@35, t10282014@27, t10242014@14, t10032014@26, t10012014@18, t09302014@13, t09222014@22, t09172014@24, t09052014@1, t08132014@16, t07302014@2, t07222014@21, t06302015@5, t06182015@4, t04102015@10, t04062015@2, t03062015@8, t03032015@1, t02102015@22, t01272015@19, t01052015@31, 03312015@14

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-0104-2016
Classification
Class II
Status
Terminated
Recall initiated
Jul 24, 2015
FDA report date
Nov 4, 2015
Quantity
1 (5mL) syringe, 1 (6mL) syringe, 18 (10mL), 1 (15mL) syringe, 3 (20mL) syringe, 3 (30mL) syringe
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-0104-2016, 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
t12312014@6, t12042014@26, t11252014@31, t10302014@35, t10282014@27, t10242014@14, t10032014@26, t10012014@18, t09302014@13, t09222014@22, t09172014@24, t09052014@1, t08132014@16, t07302014@2, t07222014@21, t06302015@5, t06182015@4, t04102015@10, t04062015@2, t03062015@8, t03032015@1, t02102015@22, t01272015@19, t01052015@31, 03312015@14
Postal code
98837-4623
Report date
Nov 4, 2015
Product type
Drugs
Recall number
D-0104-2016
Classification
Class II
Recalling firm
JD & SN Inc., dba Moses Lake Professional Pharmacy
Product quantity
1 (5mL) syringe, 1 (6mL) syringe, 18 (10mL), 1 (15mL) syringe, 3 (20mL) syringe, 3 (30mL) syringe
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
METHYLCOBALAMIN, Injectable Solution, 15 MG/ML, syringe sizes: 5 mL; 6 mL; 10 mL; 15 mL; 20 mL; 30 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-0104-2016, 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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