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. 2,453 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,453 in last 12 months

Showing 2890128920 of 49,677 recalls

Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 7.5 x 50mm screw. Part of MAXIMIS Pedicle Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Marking Pin (Round Jaw). Part of MAXIMIS Pedicle Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 300mm Straight Rod. Part of MAXIMIS Pedicle Screw Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Rod Checker. Part of MAXIMIS Pedicle Screw Spinal Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 35mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Nut Inserter B. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 5.5 mm Instrument Tap. Part of MAXIMIS Pedicle Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 80mm Curved Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 30mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Polyaxial Screw and MIS Screw Recalled by Valorem Surgical...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2017· Keystone Dental Inc

Recalled Item: Multi-Unit Abutment Angled Recalled by Keystone Dental Inc Due to Abutments...

The Issue: Abutments are unable to accept the final abutment screw

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: The firm has identified that a fitting in some Slidemaker Stainer units may...

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2017· J F C International Inc

Recalled Item: Futaba Sesame Hijiki Rice Seasoning Recalled by J F C International Inc Due...

The Issue: Firm discovered that seasoning product imported from Japan lacks an English...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 19, 2017· Leica Microsystems, Inc.

Recalled Item: Nussloch GmbH ASP6025 Tissue Processor Recalled by Leica Microsystems, Inc....

The Issue: Incorrect labeling for specified voltage for the Alarm Connectors on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2017· Nova Biomedical Corporation

Recalled Item: Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Recalled by...

The Issue: Software- scheduled A-QC analysis could initiate prior to a patient result...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2017· ConMed Corporation

Recalled Item: STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets...

The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2017· ConMed Corporation

Recalled Item: STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary Recalled by ConMed...

The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2017· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Succinylcholine Chloride Recalled by Fagron Compounding Services LLC dba...

The Issue: Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 17, 2017· House Of Thaller Inc

Recalled Item: FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g) Recalled by...

The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 17, 2017· House Of Thaller Inc

Recalled Item: LANTANA White Bean HUMMUS NET WT. 10 oz (283g) Recalled by House Of Thaller...

The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...

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

Class I — Serious Health HazardOngoing
Refund