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. 2,492 recalls have been distributed to Tennessee in the last 12 months.
Showing 28941–28960 of 52,000 recalls
Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 units added to 1000 mL 5% Dextrose/Lactated Ringer's Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 15 units added to 250 mL Lactated Ringer's Injection USP in 250 mL...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10...
The Issue: The label does not list "Sodium" in the ingredient statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10...
The Issue: The label does not list "Sodium" in the ingredient statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Recalled by DePuy...
The Issue: Leakage of FMS gravity tub sets (281113) at the bulb and tube connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling
The Issue: Potentially mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: A software update was released on August 22, 2017. Performing this software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide Recalled...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling
The Issue: Potentially mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss INTRABEAM PRS 500 Recalled by Carl Zeiss Meditec AG Due to The...
The Issue: The device had an incorrect printed calibration value on the calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Pfizer Inc. Due to...
The Issue: Presence of Particulate Matter: glass particulate found in vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.