New Jersey recalls
4195 federal recalls on file affecting New Jersey - 820 New Jersey-specific plus 3375 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-05-20FDA-DeviceStrykerClass IINationwideMedtronic Marinr catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideDaig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker Daig Livewire catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker electrophysiology catheter recalled for seal defect
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker electrophysiology catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker electrophysiology catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD EP XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD EP XT catheters recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic XT catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic XT catheters recalled for incomplete seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD Dynamic Tip Steerable recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceStrykerClass IINationwideStryker BARD catheter recalled for incomplete sterile seals
Incomplete seals on sterile product
- 2026-05-20FDA-DeviceIntegra LifeSciencesClass IINationwideCodman CerebroFlo EVD Catheter recalled for endotoxin contamination
Out-of-specification endotoxin result that did not meet the acceptance criteria.
- 2026-05-20FDA-DeviceEdwards LifesciencesClass IINationwideEdwards EVOQUE tricuspid delivery system labeling updated
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.
- 2026-05-20FDA-DeviceAniara DiagnosticaClass IINationwideAniara ZYMUTEST HIA IgG kit recalled for incorrect control values
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
- 2026-05-20FDA-DevicePhilipsClass IINationwidePhilips Azurion imaging systems recalled for cable failure risk
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or rotated.
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