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. 2,521 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,521 in last 12 months

Showing 79617980 of 47,970 recalls

Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim XR 5 Implantable Pulse Genterator (previously known Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Infinity 5 Implantable Pulse Generator Product Description: The Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Smiths Medical ASD Inc.

Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...

The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: succinylcholine Recalled by Central Admixture Pharmacy Services Inc Due to...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: morphine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: HYDROmorphone in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: morphine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: midazolam in dextrose 5% Recalled by Central Admixture Pharmacy Services Inc...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: HYDROmorphone added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: PHENYLephrine in 0.9 sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: morphine in 0.9% Sodium Chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL 2 mcg/mL and bupivacaine 0.0625% PF in 0.9% sodium chloride...

The Issue: Lack of assurance of sterility: Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund