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. 1,901 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,901 in last 12 months

Showing 2126121280 of 51,038 recalls

Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Teleflex Medical

Recalled Item: Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit...

The Issue: The safety cap attached to needles within the needle sets may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Avanos Medical, Inc.

Recalled Item: CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit Recalled by Avanos...

The Issue: The connector piece to the PEG tube does not pass over the guidewire.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2019· Avanos Medical, Inc.

Recalled Item: CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit Recalled by Avanos...

The Issue: The connector piece to the PEG tube does not pass over the guidewire.

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

Class II — Potential Health HazardOngoing
DrugOctober 7, 2019· Mylan Laboratories Limited (Sterile Products Division)

Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...

The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 7, 2019· Dole Packaged Foods, LLC

Recalled Item: Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole...

The Issue: Foreign object; potential plastic pieces.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2019· Nova Ortho-Med Inc

Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...

The Issue: Walkers within the identified serial range have the potential for the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Edwards Lifesciences, LLC

Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...

The Issue: Intermittent communication due to inconsistent crimping of connectors onto...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Implant Direct Sybron Manufacturing LLC

Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...

The Issue: Some dental implant packages contain incorrect implants, which could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Beckman Coulter, Inc.

Recalled Item: UniCel DxH Slidemaker Stainer (DxH SMS) and UniCel DxH Slidemaker Recalled...

The Issue: When the UniCel DxH Slidemaker Stainer and UniCel DxH Slidemaker Stainer II...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...

The Issue: Software issue identified in the software versions syngo CT VB20 running on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2019· Smith & Nephew, Inc.

Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...

The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...

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

Class II — Potential Health HazardOngoing
DrugOctober 4, 2019· KVK-Tech, Inc.

Recalled Item: Methylphenidate Hydrochloride Oral Solution 5mg per 5mL Recalled by...

The Issue: Presence of Foreign Substance; Fiber particles.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 4, 2019· Ventana Medical Systems Inc

Recalled Item: Model Number: 06917259001 UDI: 04015630976010 - Product Usage: The System...

The Issue: The firm became aware of a cleaning solution leaking issue from the middle...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2019· ICU Medical, Inc.

Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...

The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...

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

Class II — Potential Health HazardOngoing