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. 1,980 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,980 in last 12 months

Showing 50015020 of 47,970 recalls

DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 25, 2024· UNIMAX MEDICAL SYSTEMS INC

Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...

The Issue: The tube may fall into the surgical site during the grasping process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· Preat Corp

Recalled Item: Multiple Digital Analog Products labeled as: NobelBiocare...

The Issue: Due to a manufacturing issue, the product has a out of specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· Medtronic Xomed, Inc.

Recalled Item: NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with...

The Issue: Potential for false negative response on the NIM Vital Nerve Monitoring System

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK MINI CR-2HH-1FH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FM Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· Covidien

Recalled Item: Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT...

The Issue: Any single affected ventilator should only be used for the 10- year labelled...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK MINI CR-4HH-P Recalled by CareFusion 303, Inc. Due to Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing