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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,351 in last 12 months

Showing 2700127020 of 27,456 recalls

Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Optimum Expanse S Multiple sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Putty Multiple Sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Flex Multiple Sizes Grafton is a human bone Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Matrix PLF Multiple Sizes Grafton is a human Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2012· Osteotech Inc

Recalled Item: Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a Recalled by...

The Issue: Multiple lots of GRAFTON ¿ and XPANSE ¿, which are used for bone grafting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Spike Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary Spike Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Bacterin International, Inc.

Recalled Item: Bacterin International Recalled by Bacterin International, Inc. Due to...

The Issue: Expired product was shipped to two customers.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary Set Peristaltic Pump System...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Standard Administration Kit...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Primary VSA Stopcock Set Peristaltic...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion Pump Peristaltic Pump System designed for...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Set Peristaltic Pump System...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Secondary Administration Kit...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2012· Medrad Inc

Recalled Item: Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump...

The Issue: Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: 94" (239cm) 20 Drop Admin Set w/High Pressure 4-Way (300 psi) Stopcock...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2012· ICU Medical, Inc.

Recalled Item: High Pressure Stopcock (3-Way Recalled by ICU Medical, Inc. Due to The firm...

The Issue: The firm initiated the recall due to a molding defect in a high pressure...

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

Class II — Potential Health HazardOngoing