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. 1,082 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,082 in last 12 months

Showing 13421–13440 of 29,188 recalls

Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 91 mm Item # 195279 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 73 mm Item # 195756 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 73 mm Item # 195250 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 87 mm Item # 195278 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Interlok 75mm Item # 195275 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 63 mm Item # 195245 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 59 mm Item # 195750 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: Vanguard XP Tibial Tray 75 mm Item # 195251 Recalled by Zimmer Biomet, Inc....

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-CR Tibial Tray - Porous Plasma 91 mm Item # 195291 Recalled by Zimmer...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 65 mm Item # 195752 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Zimmer Biomet, Inc.

Recalled Item: XP-XP Tibial Tray - Interlok 79 mm Item # 195758 Recalled by Zimmer Biomet,...

The Issue: The locking bar not fully engaging

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Bioseal Corporation

Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...

The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Normand-Info S.A.S.U.

Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...

The Issue: A patch was released for a critical remote code execution vulnerability in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: Bard Conquest 40 PTA Dilation Catheter Recalled by Bard Peripheral Vascular...

The Issue: The catheter packaging incorrectly listed the balloon size as 8mm X 20mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· WOM World of Medicine AG

Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...

The Issue: The deficit displayed by the pump can differ from the real deficit, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...

The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...

The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2019· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral PDS Plus Violet 27 (70cm) CTX Needle Product Recalled by...

The Issue: The product does not meet certain internal strength testing specifications.

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

Class II — Potential Health HazardOngoing