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. 2,544 recalls have been distributed to Rhode Island in the last 12 months.
Showing 4201–4220 of 47,970 recalls
Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...
The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...
The Issue: To better define the drying procedures described in the IFU to improve the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...
The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...
The Issue: The beds have a potential for an interface issue with the Rauland Responder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...
The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atovaquone Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...
The Issue: Microbial Contamination of a Non-sterile Product: The product was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The IMAGEnet 6 Ophthalmic Data System is a software program Recalled by...
The Issue: The overlay of visual field test locations on a probability map, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use...
The Issue: A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing...
The Issue: The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.M. Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility: The...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACRI-LUBE Recalled by AbbVie Inc. Due to Lack of Assurance of Sterility:...
The Issue: Lack of Assurance of Sterility: The impacted lots may contain a breach in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phasitron5 Breathing Circuit (P5-10 Recalled by Percussionaire Corporation...
The Issue: As a result of product complaints, breathing circuits are experiencing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu¿ VivaSight 2 DLT Endobronchial tube Recalled by Ambu Inc. Due to Ambu...
The Issue: Ambu has received complaints on Ambu¿ VivaSight 2 DLTs regarding hyper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Cystoscope Outer Sheath Recalled by Olympus Corporation of the...
The Issue: Product being removed due to incompatibility when used in conjunction with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S'mores Bites Recalled by Nuts.com Due to Undeclared Allergen
The Issue: Undeclared Allergen, milk - a mix-up between the product description and the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog...
The Issue: Olympus is removing the statement of compatibility with a GreenLight Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing...
The Issue: There is a potential for pinholes in the applicator pouch film which creates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.