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. 2,669 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,669 in last 12 months

Showing 3198132000 of 55,713 recalls

Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit 2) Recalled by...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Cook Inc.

Recalled Item: Cook Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Correction...

The Issue: Correction to the product Instructions for Use because the current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arrow MAC Two-Lumen Central Venous Access Kit Introducer Catheter The...

The Issue: Arrow International is recalling the affected product because the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: Arrow Multi-Lumen CVC Kit The Arrow Two-Lumen Central Venous Access Recalled...

The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended Recalled by...

The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2017· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to Incorrect labeling; the box...

The Issue: Incorrect labeling; the box label indicates Pediatric, the product insert...

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

Class II — Potential Health HazardOngoing
DrugMay 8, 2017· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCORTISONE LOTION Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest...

The Issue: Superpotent Drug: above specification for the assay.

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

Class III — Low RiskOngoing
Refund
FoodMay 8, 2017· Fourth Street Barbeque, Inc.

Recalled Item: Pick 5 Chicken & Waffle Sandwich Recalled by Fourth Street Barbeque, Inc....

The Issue: Product has the potential to be contaminated with Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2017· RB Manufacturing LLC

Recalled Item: Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine +...

The Issue: RB Manufacturing is recalling Move Free Advance Tablets due to incorrect...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 8, 2017· Beekley Corporation

Recalled Item: Beekley Medical 0-SPOT Mammography Skin Markers Recalled by Beekley...

The Issue: Mammography Skin Marker 0 -SPOT () product was mis-labeled with A-SPOT () labels

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

Class III — Low RiskOngoing
Medical DeviceMay 8, 2017· Sterilmed Inc

Recalled Item: Electrophysiology catheter cables are designed as electrode cables with a...

The Issue: Sterilmed is recalling all lots of specific product codes of unexpired...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: When cut lines are shown on an image, the lines may go from being vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Merge PACS did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Durability characteristics of reusable instruments were not established

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

Class II — Potential Health HazardOngoing
DrugMay 5, 2017· Ascend Laboratories LLC

Recalled Item: AMLODIPINE BESYLATE TABLET Recalled by Ascend Laboratories LLC Due to...

The Issue: PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet...

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

Class III — Low RiskOngoing
Refund
DrugMay 5, 2017· Genetic Edge Compounds LLC

Recalled Item: GEC LX Laxoplex 60 capsules Dietary Supplement Recalled by Genetic Edge...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 5, 2017· Pinnacle Foods, LLC

Recalled Item: AUNT JEMIMA(R) HOMESTYLE FRENCH TOAST Recalled by Pinnacle Foods, LLC Due to...

The Issue: Potential for Listeria monocytogenes contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 5, 2017· Pinnacle Foods, LLC

Recalled Item: AUNT JEMIMA(R) FRENCH TOAST MADE WITH WHOLE GRAIN Recalled by Pinnacle...

The Issue: Potential for Listeria monocytogenes contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 5, 2017· Pinnacle Foods, LLC

Recalled Item: AUNT JEMIMA(R) 14 BLUEBERRY WAFFLES Recalled by Pinnacle Foods, LLC Due to...

The Issue: Potential for Listeria monocytogenes contamination

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

Class II — Potential Health HazardOngoing
Refund