Product Recalls in Tennessee

Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1330113320 of 29,188 recalls

Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...

The Issue: Due to low Quality Control recovery and invalid Calibration.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...

The Issue: Due to low Quality Control recovery and invalid Calibration.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 10, 2019· Novarad Corporation

Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...

The Issue: The firm received a report of an atypical dataset being generated. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Philips North America LLC

Recalled Item: Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED...

The Issue: Affected devices contain a Printed Circuit Assembly (PCA) that was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Philips North America LLC

Recalled Item: Philips HeartStart FRx AED Recalled by Philips North America LLC Due to...

The Issue: Affected devices contain a Printed Circuit Assembly (PCA) that was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· MEDTECH SAS

Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...

The Issue: The instrument holder may be sent on a trajectory that is not within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2019· Medline Industries Inc

Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...

The Issue: The recall is being conducted due to a potential defective component on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2019· CooperSurgical, Inc.

Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...

The Issue: The touchpad may not work properly after cleaning.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...

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

Class II — Potential Health HazardOngoing