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. 2,827 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,827 in last 12 months

Showing 67016720 of 53,621 recalls

Medical DeviceMarch 9, 2024· Noah Medical

Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...

The Issue: Due to a misaligned calibration of the wired controller that may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Recalled by ROUTE 92 MEDICAL INC Due to Their is the...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical Full Length 070 Access System Recalled by ROUTE 92 MEDICAL...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· ROUTE 92 MEDICAL INC

Recalled Item: Route 92 Medical 070 Reperfusion System Recalled by ROUTE 92 MEDICAL INC Due...

The Issue: Their is the potential for distal tip separation at the proximal marker band...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 8, 2024· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device:...

The Issue: Degraded and unusable upon removal from the foil pouch due to exposed...

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

Class II — Potential Health HazardOngoing
FoodMarch 7, 2024· RAJA FOODS LLC

Recalled Item: SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags Recalled by RAJA...

The Issue: Product tested positive for lead

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 7, 2024· John B. Sanfilippo & Son Inc.

Recalled Item: Great Value Honey Roasted Cashews Recalled by John B. Sanfilippo & Son Inc....

The Issue: undeclared milk and coconut

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 7, 2024· Stonewall Kitchen, LLC

Recalled Item: Stonewall Kitchen Cinnamon Sugar Doughnut Mix Recalled by Stonewall Kitchen,...

The Issue: Product contains undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Tri-Lo-Sprintec (norgestimate and ethinyl estradiol) tablets USP - triphasic...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Fresenius Kabi USA, LLC

Recalled Item: LVP Software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...

The Issue: Software has anomalies that have the potential to cause underdose, overdose,...

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

Class I — Serious Health HazardOngoing
FoodMarch 6, 2024· Colonna Brothers Inc.

Recalled Item: Supreme Tradition brand and Marcum brand ground cinnamon. Packaged in...

The Issue: Elevated lead levels in cinnamon

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2024· B. Braun Medical Inc

Recalled Item: Potassium Chloride for Injection Concentrate USP Recalled by B. Braun...

The Issue: Lack of assurance of sterility: pinholes, within the blue label characters...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2024· Artivion, Inc

Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...

The Issue: The blood cultures performed as part of the organ donation process were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Microbiologics Inc

Recalled Item: KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b Recalled by...

The Issue: The positive control material (Rhizopus stolonifer) within the KWIK-STIK...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing