Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,862 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,862 in last 12 months

Showing 21012120 of 29,496 recalls

Medical DeviceFebruary 18, 2025· CareFusion 303, Inc.

Recalled Item: BD Care Coordination Engine (CCE) Infusion Adapter Recalled by CareFusion...

The Issue: Software issue that may result in outdated automated programming...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 9 Coated Super Tampons and 9 Nude Super Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 3 Month Regular Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 18 Coated Regular Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 36 Coated Regular Tampons Recalled by DAYE (ANNE'S DAY LTD) Due...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 9 Coated Super and 9 Nude Super Tampons Recalled by DAYE (ANNE'S DAY LTD)...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 3 Month Trial Tampon Box Recalled by DAYE (ANNE'S DAY LTD) Due to...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 36 Coated Super Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Trial Tampon Box Recalled by DAYE (ANNE'S DAY LTD) Due to Product lacks...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Initiation 3 Month Regular Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: Heavy Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product lacks...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 9 Coated Regular and 9 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 18 Coated Super and 18 Nude Super Tampons Recalled by DAYE (ANNE'S DAY LTD)...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 3 Month Heavy Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2025· DAYE (ANNE'S DAY LTD)

Recalled Item: 36 Coated Super Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to Product...

The Issue: Product lacks 510(k) clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing