New York recalls
4369 federal recalls on file affecting New York - 994 New York-specific plus 3375 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-06-17FDA-DeviceAvanosClass IINationwideAvanos MIC Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for lidocaine quality issues
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos MIC Safety PEG Kit recalled for lidocaine quality issue
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO feeding tube kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanosClass IINationwideAvanos CORFLO PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO PEG kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO Safety PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO Safety PEG Kit recalled for quality defect
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceAvanos MedicalClass IINationwideAvanos CORFLO PEG Kit recalled for defective lidocaine
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
- 2026-06-17FDA-DeviceHF AcquisitionClass IINationwideSporeTraq spore testing service recalled for incubation error
Due to incorrect incubation process being performed on product.
- 2026-06-17FDA-DeviceHF AcquisitionClass IINationwideSporeTraq spore testing service recalled for incubation error
Due to incorrect incubation process being performed on product.
- 2026-06-17FDA-DeviceInspireMDClass IINationwideINSPIREMD CGuard Prime stent recalled for deployment risk
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
- 2026-06-17FDA-DeviceInspireMDClass IINationwideInspireMD CGuard Prime stent recalled for deployment risk
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
- 2026-06-17FDA-DeviceInspireMDClass IINationwideInspireMD CGuard Prime stent recalled for deployment risk
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
- 2026-06-17FDA-DeviceInspireMDClass IINationwideInspireMD CGuard Prime stent recalled for deployment risk
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
- 2026-06-17FDA-DeviceInspireMDClass IINationwideInspireMD CGuard Prime stent recalled for deployment risk
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
- 2026-06-17FDA-DeviceInspireMDClass IINationwideInspireMD CGuard Prime stent recalled for deployment risk
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
- 2026-06-17FDA-DeviceD.O.R.CClass IINationwideD.O.R.C. TDC VELOCE cutter recalled for loose outer knife
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
- 2026-06-17FDA-DeviceD.O.R.CClass IINationwideD.O.R.C. TDC VELOCE cutter recalled for loose knife risk
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
- 2026-06-17FDA-DeviceD.O.R.CClass IINationwideD.O.R.C. TDC VELOCE cutter recalled for loose knife risk
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
- 2026-06-17FDA-DeviceFresenius Medical CareClass IINationwideFresenius Bicarby Dialysate recalled for leak and slip hazard
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during manipulation of the frangible and tubing when preparing the product for use for treatment. This issue presents the potential of a slip and fall hazard associated with fluid on the floor.
- 2026-06-17FDA-DeviceBerlin HeartClass IINationwideBerlin Heart EXCOR Pediatric VAD blood pump recalled for expiration date mismatch
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
- 2026-06-17FDA-DeviceMozarc MedicalClass IINationwideMahurkar Elite PASS Trays recalled for missing dressing
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.
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