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. 2,642 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,642 in last 12 months

Showing 2854128560 of 53,621 recalls

FoodMarch 20, 2018· Pepsi Cola Bottling Company

Recalled Item: Diet Pepsi Recalled by Pepsi Cola Bottling Company Due to Case labeling...

The Issue: Case labeling (shrink-wrap labeling) for Diet Pepsi 6 packs (6-16oz bottles)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Certified Safety Mfg Inc

Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...

The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2018· Synthes, Inc.

Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...

The Issue: There is a potential for the connection screw of the stem extractor to break.

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2018· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin Capsules USP Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual...

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

Class III — Low RiskOngoing
Refund
FoodMarch 17, 2018· International Harvest, Inc.

Recalled Item: Coconut Smiles - Retail: International Harvest Brand Organic Go Smile!...

The Issue: Product tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic SEEDLESS RED RASPBERRY fruit spread NET WT Recalled by...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic STRAWBERRY fruit spread NET WT 9.5 OZ Recalled by Smucker...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Natural Grocers by Vitamin Cottage

Recalled Item: Natural Grocers Organic Coconut Smiles Recalled by Natural Grocers by...

The Issue: Coconut smiles product tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ Recalled by Smucker...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic CONCORD GRAPE fruit spread NET WT 9.5 Recalled by Smucker...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic BLACKBERRY POMEGRANATE fruit spread NET WT 9.5 Recalled...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic MANGO fruit spread NET WT 9.5 OZ Recalled by Smucker...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· NGB, Corp

Recalled Item: Nxtgen Botanicals Recalled by NGB, Corp Due to Potential Salmonella...

The Issue: NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 0.5T Standard Recalled by Philips Electronics North America...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing