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. 1,091 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,091 in last 12 months

Showing 12101–12120 of 52,000 recalls

Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress Recalled by Baxter...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Centrella Pro+ 36" Surface mattress Recalled by Baxter Healthcare...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· LumiraDx

Recalled Item: LumiraDx SARS-CoV-2 Antibody (Ab) Test Strip Recalled by LumiraDx Due to...

The Issue: Modification to the LumiraDx SARS-CoV-2 Antibody (Ab) test that was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Centrella Pro+ 40" Surface mattress Recalled by Baxter Healthcare...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress Recalled by...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress Recalled by Baxter...

The Issue: The failure mode on the affected mattresses can cause a reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· LumiraDx

Recalled Item: LumiraDx SARS-CoV-2 Antibody (Ab) Liquid Quality Control Recalled by...

The Issue: Modification to the LumiraDx SARS-CoV-2 Antibody (Ab) test that was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· GE Healthcare, LLC

Recalled Item: SIGNA Premier magnetic resonance scanner Recalled by GE Healthcare, LLC Due...

The Issue: Under rare conditions, SIGNA Premier gradient coils could result in elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Stryker Instruments

Recalled Item: Stryker 2.3mm Tapered Router Recalled by Stryker Instruments Due to There is...

The Issue: There is a potential for the core diameter to be undersized, which may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Medtronic Inc

Recalled Item: Medline Sprinter OTW Recalled by Medtronic Inc Due to Luer has balloon...

The Issue: Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Neotract Inc

Recalled Item: UroLift System Recalled by Neotract Inc Due to There is the potential that...

The Issue: There is the potential that during implant deployment, the device may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2022· Alere San Diego, Inc.

Recalled Item: The Cholestech LDX¿ System combines enzymatic methodology and solidphase...

The Issue: Cholesterol test cassettes package insert is to be updated with new...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: POLIDENT DENTURE CLEANSERS 84 CT Recalled by Family Dollar Stores, Llc. Due...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: VERIQUICK PREGNANCY TEST 1CT Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: OPTI FREE REPLENISH MULTI PURPOSE 2 OZ Recalled by Family Dollar Stores,...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: CURAD FIRST AID KIT Recalled by Family Dollar Stores, Llc. Due to Affected...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: SIMPLY SALINE NASAL MIST 3.1 OZ Recalled by Family Dollar Stores, Llc. Due...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: DENTEMP ONE STEP .077OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT Recalled by Family Dollar Stores,...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Affected product was not appropriately stored in temperature-controlled...

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

Class II — Potential Health HazardOngoing