Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,507 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,507 in last 12 months

Showing 1910119120 of 28,579 recalls

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

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ 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 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 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 MST-70 KIT Non-Valved w/ 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: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ 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: 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· 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· 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· 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
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· Interventional Spine Inc

Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...

The Issue: During implantation, the proximal end of the device could separate if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...

The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...

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

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

Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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

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

Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...

The Issue: There is a problem with the mating feature between the plate and screw which...

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