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 3020130220 of 47,970 recalls

Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA PASV 5F DL 55CM IR-145 Nitinol Wire KIT PG Recalled by Angiodynamics...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG Recalled by Angiodynamics...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Valved with Nit GW Recalled by...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA PASV 5F DL 55CM IR-145 KIT PG Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA PASV 5F DL 55CM MST-70 KIT PG Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2016· BioMerieux SA

Recalled Item: NucliSENS magnetic extraction reagents Recalled by BioMerieux SA Due to A...

The Issue: A drift of the performance with the BK test (BK virus, worst case...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 23, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Twist Drill PRO ¿4.2mm Recalled by Straumann Manufacturing, Inc....

The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Drill 1 Recalled by Straumann Manufacturing, Inc. Due to Drills...

The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2016· BioMerieux SA

Recalled Item: MagSIL (NucliSENS easyMAG Magnetic Silica) Recalled by BioMerieux SA Due to...

The Issue: A drift of the performance with the BK test (BK virus, worst case...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 23, 2016· Medline Industries Inc

Recalled Item: Unna-Z Recalled by Medline Industries Inc Due to Medline Industries, Inc is...

The Issue: Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3X10 and...

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

Class II — Potential Health HazardOngoing
FoodNovember 23, 2016· Green Dirt Farm, LLC

Recalled Item: Green Dirt Farm "Ruby" blended milk cheese packaged in cases of 6 Recalled...

The Issue: Product is contaminated with Staphylococcus aureus exceeding action limit of...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· Green Dirt Farm, LLC

Recalled Item: Green Dirt Farm "Dirt Lover" sheep's milk cheese packaged in cases of 8...

The Issue: Product is contaminated with Staphylococcus aureus exceeding action limit of...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 23, 2016· NATURECOM INC

Recalled Item: DMAA (1 Recalled by NATURECOM INC Due to Naturecom dba NutriVitaShop is...

The Issue: Naturecom dba NutriVitaShop is recalling DMAA net weight 500 g because there...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2016· HANDY SEAFOOD INCORPORATED

Recalled Item: Handy Seafood Recalled by HANDY SEAFOOD INCORPORATED Due to Handy Seafood...

The Issue: Handy Seafood states that they are initiating this recall of Blue Crab Cake...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 22, 2016· To Your Heart's Content

Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...

The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Reckitt Benckiser LLC

Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...

The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...

The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Amendia, Inc

Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...

The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...

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

Class II — Potential Health HazardOngoing