Centurion Medical Products Recalls GRIPPER Needles in Illinois
Centurion Medical Products Corporation is recalling GRIPPER Needles in Illinois. The recall was initiated by the supplier.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or specific hazards, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Centurion Medical Products Corporation is recalling GRIPPER Needles, a medical device product. The recall was initiated by the supplier.
The affected products are identified by the following lot numbers and expiration dates: 2018110501 (7/31/2021), 2018121801 (7/31/2021), 2019013001 (9/30/2021), and 2019032901 (9/30/2021). The distribution pattern indicates the products were distributed in Illinois (IL).
The source text does not specify the exact reason for the recall or the number of units affected. Consumers and healthcare providers should stop using the affected products and contact the manufacturer for further instructions.
The recalled product
- Product
- Maintenance Flush Kit/Blood Draw Product Code: DT19335
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — Needles
- Hazard
- Affected units
- 240
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 4 recalled by Centurion Medical Products Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
Same manufacturer · Centurion Medical Products Corporation
See all →- HighCenturion Difficult IV Kit Recalled for False Carboxyhemoglobin Results
FDA (Devices) · 2020-07-15
- HighCenturion ENT Snuffer Kit Recalled for Incomplete Sterile Package Seals
FDA (Devices) · 2020-02-12
- HighCenturion Medical Products Recalls Sterile Hyperalimentation and Dressing Change Trays
FDA (Devices) · 2020-02-12
- HighCenturion Chest Tube Trays Recalled for Incomplete Package Seals
FDA (Devices) · 2020-02-12
- HighCenturion Medical Products Recalls Sterile Pitcher Kits Due to Seal Defects
FDA (Devices) · 2020-02-12
Same hazard · medical device defect
See all →- HighUSTAR II Knee System Hinge Box Trial Recall
FDA (Devices) · 2026-08-12
- HighBioCera Fibers Bioresorbable Bone Void Filler Recall
FDA (Devices) · 2026-05-13
- HighHitachi Proton Beam Therapy System Recalled Due to Software Anomaly
FDA (Devices) · 2026-03-04
- HighBard Marquee Biopsy Instruments Recalled for Potential Needle Detachment
FDA (Devices) · 2024-11-27
- HighConvenience kits recalled for containing defective medical syringes
FDA (Devices) · 2024-09-25