Worldwide Notification Regarding the Recall of Jelco® Hypodermic Needle-Pro® Fixed Needle Insulin Syringe with Skewed Graduation Markings
Smiths Medical has become aware of specific models and lots of Jelco® Hypodermic Needle-Pro® Fixed Needle Insulin Syringes that may exhibit skewed odd number line graduation markings on their syringe barrels. Markings skewed approximately 20 degrees upward have been identified.
Affected Models and Lot Numbers:
|Model Number||Name||Lot Number|
|4428-1||Jelco® Hypodermic Needle-Pro® Fixed Needle Insulin Syringe 28Gx1/2” 1CC||4046543 and 4062235|
|4429-1||Jelco® Hypodermic Needle-Pro® Fixed Needle Insulin Syringe 29Gx1/2” 1CC||4014096, 4031846, 4031845, 4040734, 4043536, 4046545, 4046546, 4062239, 4062240, 4062238 and 4062242|
Please reference the below image for an illustration of the skewed graduation marking on the syringe barrel:
As a result of this issue, there is potential for administration of an incorrect dose of insulin, which could result in hyperglycemia (which may lead to ketoacidosis) or hypoglycemia (which may lead to seizures). This may result in serious harm or death.
Smiths Medical has received no reports of death or serious injury related to this issue.
Smiths Medical is issuing Recall Notices and Response Forms to consignees of Affected Models and Lot Numbers to instruct them that they must quarantine and return the product.
This action has been designated as a Class 1 recall by the U.S. Food and Drug Administration (FDA).
Home Healthcare Environments
The lot number can be found on the packaging for the syringe. Do not use any syringes with the affected lot numbers. The patient or caretaker should contact the pharmacy, home healthcare provider or medical facility that provided the syringe to arrange for return of the syringe and replacement.
Smith Medical Contact Information
Consumers with questions regarding this recall may contact Smiths Medical via telephone at 1-(800)-258-5361.
Consumers may also contact Smiths Medical online at https://smiths-medical.custhelp.com.
Specific questions on the recall should be directed to email@example.com.
FDA MedWatch Reporting
Adverse reactions or quality problems experienced with the use of these products may also be reported to the FDA’s MedWatch Program by:
- MedWatch website at www.fda.gov/medwatch
- Phone: 1-800-FDA-1033
- Fax: 1-800-FDA-0178
- Mail: MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852
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