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. 1,812 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,812 in last 12 months

Showing 2344123460 of 47,970 recalls

DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Bi-Mix Injection (Alprostadil 150 mcg/Lidocaine 2 mg/mL) Recalled by Pharm D...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Lipo MIC-12 Compound Injectable a) NDC 69699-1603-10 Recalled by Pharm D...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Phenol 7% and Glycerin Aqueous Solution 10 mL Injectable Recalled by Pharm D...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix ST-1 30PA-1.5PH-50A Aqueous Solution Pharm D Solutions Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 10, 2018· GE Healthcare Biosciences

Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...

The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· BioFire Diagnostics, LLC

Recalled Item: -Outer Kit Box (P/N RFIT-LBL-0140) - FilmArray¿ Meningitis/Encephalitis (ME)...

The Issue: Firm identified an issue in the manufacturing process which might contribute...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Howmedica Osteonics Corp.

Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...

The Issue: Potential for outer pouch sterile barrier to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: PROPONENT Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: ACCOLADE Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: ESSENTIO Pacemaker Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...

The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) Recalled by...

The Issue: Boston Scientific has identified a subset of active pacemaker and CRT-Ps...

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

Class II — Potential Health HazardOngoing
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Delivers 0.1 mg/day...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2018· Vital Scientific N.V.

Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...

The Issue: The action is being initiated because the cooling indicator board was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...

The Issue: There is lot to lot variability for QC and patient results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...

The Issue: There is lot to lot variability for QC and patient results when using the...

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

Class II — Potential Health HazardOngoing