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 22581–22600 of 27,456 recalls
Recalled Item: ASEPT Peritoneal Drainage System Recalled by Pfm Medical Inc Due to PFM...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Centesis Catheter Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Introducer Kit Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...
The Issue: A gel-like substance was found in kit component, sample diluent , that could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...
The Issue: A gel-like substance was found in kit component, sample diluent , that could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by Radiometer America Inc Due to...
The Issue: Batches of HemoCue Glucose 201 Microcuvettes show discoloration and provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...
The Issue: A gel-like substance was found in kit component, sample diluent , that could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoCool SmartTouch Navigation Catheters Recalled by Biosense Webster,...
The Issue: The recall was initiated because Biosense Webster is providing additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Neg Urine Combo Panel Type 1 Recalled by Siemens Healthcare...
The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Neg BP Combo Panel Type 3 Recalled by Siemens Healthcare Diagnostics,...
The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet...
The Issue: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...
The Issue: Cardiohelp- i System may have a software issue that can potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...
The Issue: Report received where the Align Radial Stem fractured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...
The Issue: The box of guides for a specific case arrived intact but contained two (2)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...
The Issue: The products have a wrong expiration date on their labeling, 5 years instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Intuition Distal Femoral Jig Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: Issuing a device correction because if the pin bushing is over loaded or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.