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. 2,341 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,341 in last 12 months

Showing 3316133180 of 47,970 recalls

FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: GoGo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 4, 2016· Materne North America Corp

Recalled Item: Gogo squeeZ Recalled by Materne North America Corp Due to Materne North...

The Issue: Materne North America Corp. is voluntarily recalling specific packages of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 3, 2016· Clorox Co (The)

Recalled Item: Hidden Valley Original Ranch dressing Recalled by Clorox Co (The) Due to...

The Issue: Incorrect ingredient labels inadvertently put on some bottles of salad...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 3, 2016· Dynarex Corporation

Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...

The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Roche Molecular Systems, Inc.

Recalled Item: Hand-Held Scanner USB IT3800 For sample identification and tracking when...

The Issue: The hand-held barcode scanner model IT3800 used with the COBAS AmpliPrep...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· ArthroCare Corporation

Recalled Item: TOPAZ MicroDebrider 0.8 mm Recalled by ArthroCare Corporation Due to During...

The Issue: During functional testing of devices after real time aging, it was...

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

Class II — Potential Health HazardOngoing