Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 949 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
949 in last 12 months

Showing 52281–52300 of 55,713 recalls

Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Gellhorn Flexible Pessary -2 3/4" Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Ring Flexible Pessary #4 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish Folding Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Cube Pessary 1 5/8"" Recalled by Cooper Surgical, Inc. Due...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish Folding Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Cube Pessary w/Drainage Holes #0"1" Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Gellhorn Flexible Pessary 3" Recalled by Cooper Surgical,...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Alere San Diego, Inc.

Recalled Item: IMO-402 Mononucleosis Rapid Test Device (Whole Blood/Serum/Plasma). Catalog...

The Issue: Alere San Diego is recalling the Clearview Mononucleosis Cassette because...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish w/ Support Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: LEEP REDIKIT Product No. 6060 In a Loop Electrosurgical Excision Recalled by...

The Issue: LEEP RediKit Products (for use in Loop Electrosurgical Excision Procedures)...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Furosemide Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Sodium Acetate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Cefdinir for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Defective Container: This recall is being carried out due to the potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: QUELICIN (succinylcholine chloride) Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particulate embedded in vials was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160....

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing