Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,547 recalls have been distributed to Wyoming in the last 12 months.
Showing 5361–5380 of 27,462 recalls
Recalled Item: FIXODENT ORG CREAM 2.4OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIQUICK PREGNANCY TEST 1CT Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Recalled by...
The Issue: Over-the-needle, intravascular catheters may have needles that do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DENTEMP ONE STEP .077OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor with VAMP System Recalled by Edwards Lifesciences, LLC Due...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...
The Issue: Progressa+ beds have the potential for static buildup from the casters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Products...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ Recalled by Family Dollar...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloTrac Sensor with Vamp System Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOODSENSE DENTURE CLEANSER GRN TAB 40CT Recalled by Family Dollar Stores,...
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruWave with Vamp System Pressure monitoring set Recalled by Edwards...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARC TEETH WHITENING PEN 0.06 FL OZ Recalled by Family Dollar Stores, Llc....
The Issue: Products were stored outside of labeled temperature requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acumen IQ Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...
The Issue: Their is the potential for flushing difficulties during setup of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...
The Issue: Potential for damaged and frayed power connector plug with repeated bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...
The Issue: Elevated results were detected with Li-heparin plasma samples when compared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Site M BHB Test Strips Recalled by Stanbio Laboratory, LP Due to...
The Issue: Deterioration in the stability of the Test Strips results in diminished...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coapt ControlSeal Electrode Recalled by Coapt LLC Due to Patient may...
The Issue: Patient may experience minor burn or blistering if device is exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope Recalled by Olympus Corporation...
The Issue: Sterilization failures when devices are sterilized per the Reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray Recalled...
The Issue: There is a potential for unexpected failure of the electrical components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.