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. 2,743 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,743 in last 12 months

Showing 1820118220 of 53,621 recalls

Medical DeviceDecember 7, 2020· Carl Zeiss Meditec AG

Recalled Item: IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software...

The Issue: When using software 1.90.2.09 or 1.90.8.06 and using modality worklist...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2020· VISBY MEDICAL INC

Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...

The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...

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

Class II — Potential Health HazardOngoing
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Zydus...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2020· Medela AG Medical Technology

Recalled Item: Stryker Medela .0193 AXS Universal Aspiration Tubing (01)07612367053921 -...

The Issue: Incorrect expiration date of "2023-07-24" on label of sterile tubing....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 60" (152 cm) Appx 1.9 ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 154 cm (61 IN) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18cm) APPX 0.43ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 60 IN (152cm) APPX 1.5 ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - In vitro diagnostic testing of Recalled by...

The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer - In vitro diagnostic testing of Recalled by...

The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...

The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box Recalled...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 9"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing