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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2970129720 of 55,713 recalls

Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX GSF PRECOAT SZ C-L¿ CR-FLEX GSF PRECOAT SZ C-R¿ Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CPT 12/14 COCR SIZE 1 EXT prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF)...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 6 INCH BEADED FC STEM 12X160MM LM 13X160MM LM Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
DrugNovember 28, 2017· Teva Pharmaceuticals USA

Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: high out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugNovember 28, 2017· EAI-JR286 INC

Recalled Item: Vertra Elemental Resistance (Octyl Methoxycinnamate 6% Recalled by EAI-JR286...

The Issue: CGMP Deviations: products manufactured in a manner that may impact product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 28, 2017· Alere San Diego Inc. DBA Immunalysis Corporation

Recalled Item: lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls Recalled by...

The Issue: The High (125 ng/ml) Control does not meet specification - it has been...

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

Class III — Low RiskOngoing
FoodNovember 27, 2017· H. A. R. Maspeth Corp.

Recalled Item: WOLDONG WORLD'S BEST KIMCHI WHOLE CABBAGE KIMCHI PREMIUM 3LBS (1.36kg)...

The Issue: Product contains undeclared sesame seeds.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...

The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Ethicon, Inc.

Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...

The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Recalled...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit Product Usage:...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R)...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard BLUE PLUS Pressure Injectable Quad- Lumen CVC Kit Product...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ Large-Bore Multi-Lumen CVC Kit Product Usage: The Arrow¿...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Product Usage: The Arrow¿ CVC is indicated to Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Quad- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing