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. 1,037 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
1,037 in last 12 months

Showing 15861–15880 of 47,970 recalls

FoodJanuary 21, 2021· Door County Coffee & Tea Co., Inc.

Recalled Item: Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. Recalled by...

The Issue: Retail Box did not contain list of ingredients or allergen statement.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2021· Stanley Specialty Pharmacy Compounding and Wellness Center

Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...

The Issue: Superpotent Drug. Lidocaine higher concentration than listed

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 21, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Oseltamivir Phosphate for Oral Suspension Recalled by Lupin Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications; Out-of-specification test...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Sky Medical Supplies and Equipments LLC

Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...

The Issue: Distributed COVID test kits without emergency use authorization.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· ReNovo, Inc.

Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...

The Issue: Non-sterile product was shipped to customers labelled as sterile.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Boston Scientific Corporation

Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...

The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2021· Stryker Sustainability Solutions

Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...

The Issue: Product was distributed without receiving regulatory clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2021· Smiths Medical ASD Inc.

Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Smiths Medical became aware that three lot numbers of a specific model of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Biomet, Inc.

Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...

The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...

The Issue: Locking mechanism has been observed to disassociate either intraoperatively...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2021· Medtronic Vascular

Recalled Item: Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375...

The Issue: Sterility may be compromised due to an unsealed pouch

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

Class II — Potential Health HazardOngoing