Z-3202-2018Class II

Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are...

Name: Z-3202-2018 Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are...
Creator: ShinChang Medical Co., Ltd.
Published: 2018-08-24
License: https://open.fda.gov/license/

ShinChang Medical Co., Ltd. / initiated 2018-08-24 / Terminated

FDA source

ShinChang Medical Co., Ltd. began a recall of Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are packaged in a flexible plastic (poly bag) and 10... on 2018-08-24. FDA classified it as Class II and gives the reason as "Defect consists of a small crack in the top end of the barrel near the needle". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-3202-2018
Classification: Class II
Status: Terminated
Initiated: 2018-08-24
Posted: 2018-09-20
Terminated: 2023-01-04
Recalling firm: ShinChang Medical Co., Ltd.
Product: Disposable Insulin Syringe 0.3mL in 3 different sizes 29Gx1/2, 30Gx5/16, and 31G x 5/16. (10 syringes are packaged in a flexible plastic (poly bag) and 10 flexible plastic (poly bag) are packaged in one in box. Finally, pack the inboxes in the carton case.)
Product code: FMF Syringe, Piston
Reason for recall: Defect consists of a small crack in the top end of the barrel near the needle.
FDA root cause: Under Investigation by firm
Action: The company has been requesting that the importers immediately cease all distribution of affected Lot Numbers and notify its customers to do the same. The customers shall include wholesale distributors, retail pharmacies and mail order pharmacies or patients. The customer who received the affected products shall quarantine. The customers may return the affected products and the company will replace. Any and all questions pertaining to the recall and disposition of recalled product can be addressed to Yushin Kim, CEO ShinChang Medical Co.,Ltd. By email at [email protected] or by phone at +82-54-463-2400
Quantity in commerce: 6,570,800
Distribution: FL, TN, and VA
Product codes and lots: GNP Insulin Syringe 0.3mL 31G¿5/16" NP18127, Healthmart Insulin Syringe 0.3mL 31G¿5/16" NP18155, Healthmart Insulin Syringe 0.3mL 31G¿5/16" NP18186, Kroger Insulin Syringe 0.3mL 30G¿5/16" NP18082, Kroger Insulin Syringe 0.3mL 31G¿5/16" NP18083, Kroger Insulin Syringe 0.3mL 30G¿5/16" NP18126, Kroger Insulin Syringe 0.3mL 30G¿5/16" NP18146, Kroger Insulin Syringe 0.3mL 31G¿5/16" NP18157, Leader Insulin Syringe 0.3mL 31G¿5/16" NP18123, Leader Insulin Syringe 0.3mL 31G¿5/16" NP18130, Leader Insulin Syringe 0.3mL 30G¿5/16" NP18151, Leader Insulin Syringe 0.3mL 31G¿5/16" NP18161, Leader Insulin Syringe 0.3mL 30G¿5/16" NP18180, Leader Insulin Syringe 0.3mL 31G¿5/16" NP18202, Nipro Insulin Syringe 0.3mL 31G¿5/16" NP18125. Nipro Insulin Syringe 0.3mL 30G¿5/16" NP18129. Nipro Insulin Syringe 0.3mL 31G¿5/16" NP18142. Nipro Insulin Syringe 0.3mL 31G¿5/16" NP18170. Nipro Insulin Syringe 0.3mL 29G¿1/2" NP18196. Nipro Insulin Syringe 0.3mL 30G¿5/16" NP18197. Nipro Insulin Syringe 0.3mL 30G¿5/16" NP18199. Sunmark Insulin Syringe 0.3mL 31G¿5/16" NP18124, Sunmark Insulin Syringe 0.3mL 30G¿5/16" NP18128, Sunmark Insulin Syringe 0.3mL 31G¿5/16" NP18136, Sunmark Insulin Syringe 0.3mL 31G¿5/16" NP18166, Sunmark Insulin Syringe 0.3mL 30G¿5/16" NP18206, Lite Touch Insulin Syringe 0.3mL 30G¿5/16" LT1805, and McKesson Insulin Syringe 0.3mL 31G¿5/16" KSH0603.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-3202-2018
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-3202-2018	Class II	Terminated	Voluntary: Firm initiated	2018-09-26	2018-09-20

Product code FMF

K993017Class IIProfi Disposable Syringe, Profi Disposable Needle, Dm Ject Insulin SyringeShinchang Medical Co., Ltd. / cleared 2000-02-25

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)