Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,489 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,489 in last 12 months

Showing 1386113880 of 27,456 recalls

Medical DeviceApril 10, 2019· Becton Dickinson & Company

Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...

The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...

The Issue: Product with incorrect shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...

The Issue: Product with incorrect shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount Recalled...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Recalled by...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· DePuy Spine, Inc.

Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...

The Issue: A complaint trend was observed for post-operative loss of height and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· DePuy Spine, Inc.

Recalled Item: Concorde Lift Recalled by DePuy Spine, Inc. Due to A complaint trend was...

The Issue: A complaint trend was observed for post-operative loss of height and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Potential loose cable connections on the reagent cooler, which could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2019· Advanced Bionics, LLC

Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...

The Issue: The manufacturer received complaints that customers were attempting to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing
Medical DeviceApril 4, 2019· Roche Diagnostics Corporation

Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...

The Issue: There is a potential for the tray input flap on the post analytical units to...

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

Class III — Low RiskOngoing