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. 2,830 recalls have been distributed to Texas in the last 12 months.
Showing 11701–11720 of 55,713 recalls
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Electrocardiograph Recalled by Baxter Healthcare Corporation Due to...
The Issue: One ELI 380 Electrocardiograph intended to be used for a pilot program was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak Surgical Procedure Pack Recalled by Alcon Research, LLC Due...
The Issue: Due to difficulty removing the liner on the adhesive components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0. Used to display medical images (Including...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0. Used to display...
The Issue: There is the potential that after installation of the IAS tool, some studies...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BabyBel Snacker (FG0401 SW Snacker ACABB 5pk) Crunch Pak 5.75 Recalled by...
The Issue: Allergens of almonds and milk not declared on the product ingredient label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gourmet Old-Fashioned Caramel Holiday Popcorn Recalled by Rieckhoff Family...
The Issue: Label contains "Gluten Free" claim but product contains wheat and barley...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CytoCell BCL11B Proximal in FITC Spectrum-LDT for investigation T-cell...
The Issue: Device is mislabeled. The package insert for this ASR device contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoCell BCL11B Distal in Texas Red Spectrum- Analyte Specific Reagent...
The Issue: An error with the chromomap on version 1 of the package insert which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE Recalled by...
The Issue: Upon review of its batch record, Southmedic identified that lot # W92761 was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic...
The Issue: Confirmed an average positive bias of 40% for testosterone concentrations of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrackX Insight Base Modular Instrument Tracker Recalled by Trackx Technology...
The Issue: The device is breaking and falling off the Nuvasive T-Handle with Hudson...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...
The Issue: The products may have the potential to burn customers. Firm has received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infection Control (IC) Lifting Strap used with the following Cirrus Recalled...
The Issue: Two customers reported four incidents in which the lifting strap broke while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Viatris Inc Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: Tablets exceeds specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1...
The Issue: Potential table stop due to a broken tabletop cable: On the ProxiDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.