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. 2,115 recalls have been distributed to Tennessee in the last 12 months.
Showing 3021–3040 of 52,000 recalls
Recalled Item: Otopore Cylinder Standard outer ear dressings Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 8cm nasal/sinus temporary wound dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore FD fragmentable nasal dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nasopore 4cm fragmentable nasal dressing Recalled by Stryker Corporation Due...
The Issue: There is a potential for blister seals on the product to present a bubble on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed Surfaces Recalled by Baxter Healthcare Corporation Due to The...
The Issue: The air bladders inside the mattress may move out of position when the head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...
The Issue: Chemical Contamination: Presence of benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CINNABON CLASSIC CINNAMON ROLL INTERNATIONAL delight COFFEE CREAMER 32 FL...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) Recalled by...
The Issue: The firm received complaints of spoilage and illness with the use of the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...
The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.