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. 2,879 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,879 in last 12 months

Showing 141160 of 53,621 recalls

Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Dynarex Recalled by ACME UNITED CORPORATION Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 20, 2026· ACME UNITED CORPORATION

Recalled Item: Med Nap BZK Antiseptic Towelettes (Benzalkonium Chloride 0.13%) Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 PAK Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Urine Albumin (UAlb). Material Number: 11537225 Recalled by...

The Issue: Falsely depressed UAlb patient results may occur. Affected samples with any...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2026· Instrumentation Laboratory

Recalled Item: GEM Premier 5000 Recalled by Instrumentation Laboratory Due to Confirmed...

The Issue: Confirmed customer complaints indicating that GEM PAKs (cartridges) for the...

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

Class II — Potential Health HazardOngoing
FoodJanuary 17, 2026· Palmetto Gourmet Foods Inc.

Recalled Item: VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients:...

The Issue: Product contains undeclared Yellow #5

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 17, 2026· Palmetto Gourmet Foods Inc.

Recalled Item: VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients:...

The Issue: Product contains undeclared Yellow #5

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2026· McKesson

Recalled Item: UDENYCA Recalled by McKesson Due to Temperature Abuse. 116 cartons with...

The Issue: Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2026· GE Healthcare

Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Client Recalled by...

The Issue: Under certain workflows, patient information shown in the viewer may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for Recalled...

The Issue: Issue with software algorithm which may lead to overpressure events.

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

Class I — Serious Health HazardOngoing
FoodJanuary 16, 2026· Bader Enterprises, Inc.

Recalled Item: Premium Food Bubble Gum Recalled by Bader Enterprises, Inc. Due to...

The Issue: Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2026· Olympus Corporation of the Americas

Recalled Item: Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for Recalled...

The Issue: Issue with software algorithm which may lead to overpressure events.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2026· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Private Label CVS. Model Number: CVS405406. Helps maintain a moist Recalled...

The Issue: Potential packaging failures, which could lead to a breach in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2026· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers:...

The Issue: Potential packaging failures, which could lead to a breach in the sterile...

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

Class II — Potential Health HazardOngoing