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. 2,368 recalls have been distributed to Rhode Island in the last 12 months.
Showing 23061–23080 of 47,970 recalls
Recalled Item: Testosterone 200mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 15mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 6 mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 10mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cedar's Chickpea Salad Recalled by Cedar's Mediterranean Foods, Inc. Due to...
The Issue: Product may contain undeclared edamame (soy).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Tomato & Basil Hummus Dip Recalled by Bakkavor Foods USA, Inc....
The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Hummus quartet Recalled by Bakkavor Foods USA, Inc. Due to...
The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...
The Issue: software malfunction; It was found when a user performs radiography using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...
The Issue: Potential that gauze pads may not be fully sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.