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. 1,034 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
1,034 in last 12 months

Showing 23201–23220 of 52,000 recalls

Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance PICC Product Code: CDC45541HPK1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC powered by Arrow VPS Stylet Product Code: ASK45041JHVA Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45052 HPK1A...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC with Chlorag+ard¿ Technology Product Code: PR 45541 HPHNL...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42063 HPHNM...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard Technology Product Code: JR 42541 HPHNM...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC with Chlorag+ard Technology Product Code: CDC 44052 HPK1A...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC with Chlorag+ard¿ Technology Product Code:PR 45552 HPHNM...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: JRT 43552 HPHNM Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 41541 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code:CDC 42052 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC Kit pre loaded with Arrow¿ VPS Precision Stylet Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: JRT 43541 HPHNM Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
DrugApril 23, 2019· D.B.P. Distribution

Recalled Item: Titanium 4000 Recalled by D.B.P. Distribution Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 23, 2019· Akorn Inc

Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...

The Issue: Failed impurities/degradation specification: Out of Specification result for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 22, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Unison Hand Care Products Recalled by Inopak Ltd Due to CGMP Deviations:...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap Recalled by Inopak Ltd Due to CGMP Deviations: hand...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 22, 2019· Inopak Ltd

Recalled Item: INOFOAM Foaming E-2 Food Handling Wash with .6% PCMX Recalled by Inopak Ltd...

The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund