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. 2,683 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,683 in last 12 months

Showing 2282122840 of 53,621 recalls

Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· MOTEK MEDICAL B.V.

Recalled Item: Body Weight Support (BWS) Light Recalled by MOTEK MEDICAL B.V. Due to The...

The Issue: The firm discovered a potential manufacturing deviation of the yoke of the...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2019· Aurobindo Pharma USA Inc.

Recalled Item: Simvastatin Tablets Recalled by Aurobindo Pharma USA Inc. Due to Labeling;...

The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; some bottles labeled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJuly 29, 2019· Upsher Smith Laboratories, Inc.

Recalled Item: Bexarotene Capsules Recalled by Upsher Smith Laboratories, Inc. Due to...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted Sidekick Floor Stand Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted IRC Display Recalled by Medtech Products, Inc. Due to...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Hand Pocket Pal Tray Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund