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. 1,742 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
1,742 in last 12 months

Showing 4492144940 of 51,038 recalls

Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 20MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 5MM X 30MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 5MM X 15MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand GDC-18 360 18MM X 30CM Recalled by Stryker Neurovascular Due...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 150CM 2 TIP Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand GDC-10 ULTRA SOFT 2MM X 3CM Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand SUPER COMPLIANT 7MM X 15MM Recalled by Stryker Neurovascular...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Zimmer, Inc.

Recalled Item: Palacos¿ R+G Radioplaque Bone Cement 1 x 40 g Single (with Gentamicin)...

The Issue: The patient label associated with the product may be incorrect in that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED J 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Medline Industries Inc

Recalled Item: Mucus Specimen Trap 40 cc Recalled by Medline Industries Inc Due to There is...

The Issue: There is a potential that the specified mucus specimen traps are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 45 150CM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 30MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand COMPLIANT 4MM X 10MM Recalled by Stryker Neurovascular Due to...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Acetabular Pressurizer Recalled by Stryker Instruments Div. of Stryker...

The Issue: On March 14, 2013 a Work Order was opened for 120 units (20 boxes) of the...

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

Class II — Potential Health HazardOngoing
DrugNovember 1, 2013· Greenstone Llc

Recalled Item: Nifedipine Recalled by Greenstone Llc Due to Labeling: Incorrect or Missing...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· Sigma-Tau Pharmaceuticals, Inc.

Recalled Item: PEGASPARGASE ONCASPAR Injection Recalled by Sigma-Tau Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Sigma-Tau PharmaSource, Inc. is conducting a...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund