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.
Showing 26981–27000 of 30,921 recalls
Recalled Item: Oxoid Vancomycin 30 mcg Recalled by Remel Inc Due to Some of the discs may...
The Issue: Some of the discs may not be impregnated with the antibiotic.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: A component of the MRx Processor Board may be susceptible to damage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M3536A HeartStart MRx with Wireless Link Upgrade (861289) The HeartStart...
The Issue: Wireless Link may be unable to transmit data when configured for a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...
The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...
The Issue: There are two situations that may occur when using the GemStar Docking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...
The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...
The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...
The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11...
The Issue: Spacelabs has voluntarily recalled G2 Clinical Access Software CD because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT580/Discovery CT590RT scanners running software...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips HeartStart XL may experience a power board failure causing failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySearch Ray Station Radiation Therapy Treatment Planning System Recalled...
The Issue: RaySearch Laboratories has recalled "RaySearch Ray Station 2.0, 2.5, 3.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8. It is intended to be used Recalled by Zimmer...
The Issue: An undetected shift between the information displayed in the navigation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Intact PTH Controls consists of 3 x 1 Bottle Recalled by Abbott...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Intact PTH Calibrators consists of 6 bottles (4.0 mL Recalled by...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synthes Hohmann Retractor Recalled by Synthes, Inc. Due to The Synthes...
The Issue: The Synthes Hohmann Retractor was mis-etched on the product and package as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS BUN UREA NITROGEN For the In vitro quantitative determination Recalled...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AST For the In vitro quantitative determination of AST Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.