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. 1,017 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
1,017 in last 12 months

Showing 37061–37080 of 53,621 recalls

Medical DeviceApril 6, 2016· Pentax Medical Company

Recalled Item: Duodenoscope Product Usage: Intended to provide optical visualization of and...

The Issue: Pentax Medical Video Processor EPK-i5010 has been shipped with a reusable...

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

Class II — Potential Health HazardOngoing
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 705000 IQF 3/8" Dice Yellow Onion Recalled by Oregon Potato Company Due to...

The Issue: 3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4" Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 1/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 3/8" White Onion Dice- FRESH Recalled by Oregon Potato Company Due to...

The Issue: 3/8" White Onion Dice- FRESH is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/8" Yellow Onion Strip Recalled by Oregon Potato Company Due to...

The Issue: IQF 3/8" Frozen Yellow Onion Strip and IQF 3/8" Yellow ORGANIC Onion Strip...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/4" Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 3/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 3/8" Un-Blanched Yellow Onion Dice Recalled by Oregon Potato Company Due...

The Issue: IQF 3/8" Un-Blanched, Frozen, Yellow Onion Dice is voluntarily recalled...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4 x 1/4 Yellow Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: 1/4 x 1/4 Frozen Yellow Onion Dice was voluntarily recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: 3/8" White Onion Strip-FRESH Recalled by Oregon Potato Company Due to...

The Issue: 3/8" White Onion Strip-FRESH was voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2016· Oregon Potato Company

Recalled Item: IQF 1/4" Frozen WHITE Onion Dice Recalled by Oregon Potato Company Due to...

The Issue: IQF 1/4" White Onion Dice is voluntarily recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 5, 2016· Empirical Laboratories, Incorporated

Recalled Item: Liposomal Magnesium Nutritional Supplement. 6 FL. OZ (180 ml) The Recalled...

The Issue: Empirical Labs is recalling Liposomal Magnesium because of the potential for...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2016· Fresenius Kabi USA, LLC

Recalled Item: Cisatracurium Besylate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Incorrect/ Undeclared Excipient: Firm is recalling product due to an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 5, 2016· Ceg Enterprises Llc

Recalled Item: Germ Terminator Recalled by Ceg Enterprises Llc Due to CEG Enterprises, LLC...

The Issue: CEG Enterprises, LLC is recalling Germ Terminator Toothbrush Sanitizer GT100...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Masimo SPO2 Sensor Recalled by Merge Healthcare, Inc. Due to Under certain...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...

The Issue: When taking measurements from images on the Cardio workstation or from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: SpO2 connecting cable for Masimo LNCS sensor (Merge Part Number:...

The Issue: Under certain conditions, the cables used with the Hemo system during a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive when used with RadSuite. The firm name Recalled...

The Issue: The software produced a number of "do not route" exceptions, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Enterprise Archive (ICEA) software. The firm name on the Recalled...

The Issue: An error message can occur resulting in the prior studies being unavailable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare....

The Issue: Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Care Systems Recalled by Merge Healthcare, Inc. Due to The system...

The Issue: The system will completely stop allowing the downloading or acquisition of...

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

Class II — Potential Health HazardOngoing