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. 2,407 recalls have been distributed to Tennessee in the last 12 months.
Showing 2361–2380 of 29,188 recalls
Recalled Item: Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT Recalled...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL Recalled...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY Recalled by MEDLINE...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alteon XLE Item Number / Product Description: 140-22-70 NV EHXL Recalled by...
The Issue: Due to the lack of the Ethylene Vinyl Alcohol (EVOH) barrier layer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeiMed NasoGel for DRY NOSES UDI-DI/code: 00705928045309 SKU...
The Issue: Due to nasal spray stability failure for bioburden.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System Recalled by Accuray Incorporated Due to...
The Issue: Snap rings may become partially or completed detached from the shafts within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...
The Issue: Due to internal venturi component getting transiently stuck in the forward...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE Polypropylene Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Solution Set with Duo-Vent Spike Recalled by Baxter Healthcare...
The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...
The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Recalled by Randox...
The Issue: Lipoprotein (a) on Roche Cobas c501 with nmol/l claims does not have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breathe Technologies Recalled by Baxter Healthcare Corporation Due to There...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Continu-Flo Solution Set with Duo-Vent Spike Recalled by Baxter...
The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number:...
The Issue: Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.