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. 2,504 recalls have been distributed to Tennessee in the last 12 months.
Showing 24581–24600 of 52,000 recalls
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoSpan SuperElastic Compression Staple w/Instruments Recalled by In2bones...
The Issue: The NeoSpan Compression Staple (10x10x10) kits from two lots contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow CVC 2 Lumen Recalled by Arrow International Inc Due to The lidstock...
The Issue: The lidstock states the incorrect priming volume and flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot¿ LA () The Staclot¿ LA and Staclot¿ LA Recalled by Diagnostica...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot LA 20 () The Staclot¿ LA and Staclot¿ Recalled by Diagnostica Stago,...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quetiapine Tablets USP 400 mg Recalled by Ascend Laboratories LLC Due to...
The Issue: Presence of Foreign Substance; metal shard found in tablet
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Raindrop Near Vision Inlay Recalled by RVO 2.0, INC Due to During a post...
The Issue: During a post approval study the firm found there was an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDS Light Suspension Recalled by Stryker Communications Due to There is a...
The Issue: There is a potential the joint in the suspension of the device is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux,...
The Issue: The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for...
The Issue: Insufficient seal on the sterile barrier of the device, compromising the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to Isocenter shifts...
The Issue: Isocenter shifts when using dose tracking in RayStation 3.5, RayStation 4.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion Pack Recalled by LivaNova USA Due to 4-way stopcocks and stopcock...
The Issue: 4-way stopcocks and stopcock manifold assembled in certain perfusion tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by AMERICAN...
The Issue: Cross contamination with other products: This sub-recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equi-Soft Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medi-Stat Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Best Taste Brand DRIED BAMBOO SHOOT Mang Non. The product Recalled by...
The Issue: Product contains undeclared sulfites (75 mg per serving).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 09076 / Recalled...
The Issue: Possible contamination with cleaning chemicals.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz. Recalled by...
The Issue: One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ERBITUX CETUXIMAB Injection Recalled by Eli Lilly & Co Due to Labeling:...
The Issue: Labeling: Missing label; potential for missing primary container label on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled...
The Issue: Unintentional U-Arm movement
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.