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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,560 in last 12 months

Showing 25212540 of 47,970 recalls

Medical DeviceApril 7, 2025· Ambu Inc.

Recalled Item: Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US...

The Issue: Incorrect labeling in which the front red pouch label did not match the...

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

Class II — Potential Health HazardOngoing
FoodApril 4, 2025· Duda Farm Fresh Foods, Inc.

Recalled Item: Marketside brand celery stick. Net wt. 1.6 OZ. (45g) Recalled by Duda Farm...

The Issue: Product tested positive for Listeria Monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 4, 2025· Klinika Mdical Gmb

Recalled Item: KliniTray Platte Faxitron Recalled by Klinika Mdical Gmb Due to Potential...

The Issue: Potential for microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2025· Klinika Mdical Gmb

Recalled Item: KliniTray. KlinioTray. Tissue resection margin examination board/small....

The Issue: Potential for microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Recalled by Integra LifeSciences...

The Issue: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...

The Issue: Preset treatment parameters are not consistently being used in accordance...

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

Class II — Potential Health HazardOngoing
DrugApril 3, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...

The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Medtronic Neuromodulation

Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...

The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Globus Medical, Inc.

Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...

The Issue: Devices for the affected lot were not assembled according to product...

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

Class II — Potential Health HazardOngoing
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 2, 2025· Preat Corp

Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...

The Issue: Due to manufacturing issues, abutment products were manufactured with screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2025· Getinge Disinfection Ab

Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...

The Issue: The frequency inverter is not programmed by supplier according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2025· Getinge Disinfection Ab

Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...

The Issue: The frequency inverter is not programmed by supplier according to...

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

Class II — Potential Health HazardOngoing
FoodApril 1, 2025· Panaderia Salvadorena Ii

Recalled Item: PANADERIA/BAKERY Salvadorena Recalled by Panaderia Salvadorena Ii Due to...

The Issue: Product contains undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund