Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,636 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,636 in last 12 months

Showing 62816300 of 51,038 recalls

DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Weiner Boner Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Flower Power Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Pink Pussycat Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Spanish Fly 22K capsules Recalled by Pyramids Wholesale Inc. Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: Samurai-X Honey 6800 Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: ALPHASTRIP MALE PERFORMANCE ENHANCER Recalled by Pyramids Wholesale Inc. Due...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: HONEY MANUKA BUNNY LOVE Recalled by Pyramids Wholesale Inc. Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: SILVERBACK XXX POWER MALE ENHANCEMENT Recalled by Pyramids Wholesale Inc....

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: The GOAT SUBLINGUAL STRIP Recalled by Pyramids Wholesale Inc. Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: libigrow RED DRAGON+ Recalled by Pyramids Wholesale Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2024· Pyramids Wholesale Inc.

Recalled Item: GoHARD 25000 Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 19, 2024· TriMed Inc.

Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...

The Issue: Nail system contains an out of specification driver-socket which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2024· TriMed Inc.

Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...

The Issue: Nail system contains an out of specification driver-socket which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: LifeVentEVO2 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Aeris EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Garbin EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing