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 92219240 of 47,970 recalls

DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-102 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-101 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: Gelson's Sea Salt Pretzels Recalled by Dakota Style, Inc Due to Undeclared Milk

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: 1. Hy-Vee Salt & Vinegar Braided Pretzels Recalled by Dakota Style, Inc Due...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: 1. Hy-Vee Dill Pickle Braided Pretzels Recalled by Dakota Style, Inc Due to...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: 1. Hy-Vee Honey Mustard Braided Pretzels Recalled by Dakota Style, Inc Due...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...

The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...

The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2023· TELEFLEX LLC

Recalled Item: Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat...

The Issue: The product contains an expired diluent vial. If the impacted product is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2023· Spacelabs Healthcare, Inc.

Recalled Item: Ultraview SL (UVSL) Command Module Recalled by Spacelabs Healthcare, Inc....

The Issue: Command modules will display the following when parameter processing is...

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

Class II — Potential Health HazardOngoing
DrugApril 11, 2023· Sanofi-Aventis U.S. LLC

Recalled Item: Admelog Recalled by Sanofi-Aventis U.S. LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Malformed crimped collar seal

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2023· Medtronic Navigation, Inc.

Recalled Item: StealthStation Cranial Software Recalled by Medtronic Navigation, Inc. Due...

The Issue: During non-axial/some axial exams, software anomalies occur during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: Recalled by Bard...

The Issue: Coaxial cannula internal diameter and length of biopsy instruments exceed...

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

Class II — Potential Health HazardOngoing
DrugApril 10, 2023· SCA Pharmaceuticals

Recalled Item: Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL Recalled by SCA...

The Issue: Subpotent Drug: Out of specification results for low potency was obtained.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 10, 2023· Keystone Industries

Recalled Item: Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture...

The Issue: The Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as...

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

Class II — Potential Health HazardOngoing