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. 2,603 recalls have been distributed to New Jersey in the last 12 months.
Showing 38941–38960 of 53,621 recalls
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Product recalled due to reports of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Recalled by Pine...
The Issue: Presence of particulate matter: Presence of silicone oil microdroplets in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD 3.2 CLI DL380 Product Usage: MYLA is Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 ML350 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.1 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 OR Table Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH3000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH5000 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...
The Issue: Procedure Products initiated the recall due to the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 9 (biplane) Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.