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. 2,586 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,586 in last 12 months

Showing 4270142720 of 53,621 recalls

Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2015· Teleflex Medical

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
FoodJanuary 13, 2015· Gilster-Mary Lee Corp.

Recalled Item: Honey & Oat Mixers ready-to-eat dry cereal sold under the Recalled by...

The Issue: Undeclared almonds

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 13, 2015· Teleflex Medical

Recalled Item: LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5 Recalled by Teleflex...

The Issue: The labelling of units from the affected lot indicates that it contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Medtronic Sofamor Danek USA Inc

Recalled Item: KYPHON EXPRESS Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The product, labeled as containing, one bevel-tipped instrument and one...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion set due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System...

The Issue: In case of a system crash, images may not be written to the hard disk and...

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

Class II — Potential Health HazardOngoing
DrugJanuary 12, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...

The Issue: Defective Delivery System: One lot exceeded the mechanical peel specification

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2015· Zenobia Company LLC

Recalled Item: My Spice Sage CUMIN GROUND under the following labels and Recalled by...

The Issue: Cumin may contain undeclared peanut protein.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 12, 2015· HVL, LLC

Recalled Item: Melatonin Control- Released Tablets Recalled by HVL, LLC Due to Bottles...

The Issue: Bottles contained a vegetarian digestive enzyme dietary supplement instead...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 12, 2015· La Flor Products Co., Inc.

Recalled Item: La Flor ground COMINO Recalled by La Flor Products Co., Inc. Due to...

The Issue: Product may contain undeclared peanut protein.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 12, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Servo-I ventilator system CO2 analyzer. Part number 65 23 588. Recalled by...

The Issue: A calibration problem was detected in a specific number of the Servo-I...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 12, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Puritan Bennett 980 Ventilator System Recalled by Covidien LP (formerly...

The Issue: Covidien is issuing a voluntary field action for all Puritan Bennett 980...

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

Class II — Potential Health HazardOngoing
FoodJanuary 9, 2015· Nu Products Seasoning Co.

Recalled Item: NuSpice Taco Seasoning - F4422 D Recalled by Nu Products Seasoning Co. Due...

The Issue: Nu Products Seasoning Product is recalling their F4422 Taco Seasoning may be...

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

Class I — Serious Health HazardOngoing
Refund