NES Recalls

2 recalls found for NES. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre

Northeast Scientific Corp. recalled 1,019 units of the NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter. The model is not cleared for marketing in the United States. The recall cites potential breaches in sterile barrier packaging that could compromise sterility. Patients and healthcare providers should stop using the device immediately. Follow the manufacturer's recall instructions

Northeast Scientific
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter Recall: 616 Units In US Distribution

Northeast Scientific Inc. has issued a recall for 616 units of the NES Reprocessed Turbo-Elite Laser Atherectomy Catheter, Model R-417-156. The FDA-listed recall cites breaches in sterile barrier packaging that could compromise sterility. The devices were distributed nationwide in the United States to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, and VA. Patients should not be in

Northeast Scientific
Potential for
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Brand Statistics

Total Recalls
2
Pages
1

Related Brands

Northeast Scientific
    NES Recalls | RecallRadar