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. 2,664 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,664 in last 12 months

Showing 29412960 of 28,245 recalls

Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1/2X6 Model/Catalog Number: 801451. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1/8X6 Model/Catalog Number: 801449. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X1/2 Model/Catalog Number: 801400. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3/4X6 Model/Catalog Number: 801452. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 2X6 Model/Catalog Number: 801455. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3X6 Model/Catalog Number: 801456. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/4X3 Model/Catalog Number: 801398. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3-1/2X6 Model/Catalog Number:801457. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X1 Model/Catalog Number: 801402. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: MICR PATIE RND Model/Catalog Number: 801396. CODMAN Surgical Patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/4X1-1/2 Model/Catalog Number: 801397. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X3 Model/Catalog Number: 801407. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1/4X6 Model/Catalog Number: 801450. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1X1 Model/Catalog Number: 801403. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Covidien LP

Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...

The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...

The Issue: To better define the drying procedures described in the IFU to improve the...

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

Class II — Potential Health HazardOngoing