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. 2,658 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,658 in last 12 months

Showing 2390123920 of 53,621 recalls

Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer with PACS-IW foundation 6.0 Recalled by GE...

The Issue: There is a potential that one or more images or image series may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Arrow International Inc

Recalled Item: Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip...

The Issue: Lidstock contains a labeling error. The lidstock shows the catheter cross...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD Recalled by Covidien LLC Due...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Power Express Sample Processing System AU5800XL connection...

The Issue: Potential exposure to biohazard. Software design problem causes excess speed...

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

Class II — Potential Health HazardOngoing
FoodMay 17, 2019· House of Spices India, Inc.

Recalled Item: Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch Code: 2324617054...

The Issue: Product contains elevated levels of undeclared Sulfites

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: GE Pristina Serena - Product Usage: Pristina Serena is an Recalled by GE...

The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: GE Senographe Pristina - Product Usage: Senographe Pristina generates...

The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...

The Issue: There is the possibility of viewing studies directly from the Enterprise...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Is a device that displays medical Recalled...

The Issue: There is the possibility of viewing studies directly from the Enterprise...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C...

The Issue: Observed reported incidence rate for harm associated with intraoperative...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C...

The Issue: Observed reported incidence rate for harm associated with intraoperative...

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

Class II — Potential Health HazardOngoing