Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,482 recalls have been distributed to Utah in the last 12 months.
Showing 22301–22320 of 28,579 recalls
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential exists for order transactions from interfaced HIS (Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System (enGen System) Recalled by Ortho-Clinical...
The Issue: Recapper Caps may fall off of, or be knocked from sample tubes placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75....
The Issue: The product failed to meet the internal established statistical test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device Recalled by...
The Issue: Potential device damage on the strain relief near the hub area, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator....
The Issue: The Astral device allows clinicians to disable all alarms including those...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to under...
The Issue: under certain circumstances the Cios Alpha system may freeze during a procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Avant Garde Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential safety risk of collision of the LINAC gantry with the patient or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Wave Access Kit Recalled by Spine Wave, Inc. Due to Mislabeling
The Issue: Mislabeled outer carton: Monopolar Probe is listed as 200 x 1.5mm when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigation System II-Cart Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker initiated a device recall of the Navigation System II-Cart, Camera...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Volume Extension Set Recalled by Smiths Medical Asd Inc Due to Smiths...
The Issue: Smiths Medical has become aware of an issue with the Low Volume Extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unilateral external fixation ankle clamp Product Usage: Unilateral external...
The Issue: Ankle clamp was assembled incorrectly; the offset of the pin to the pivot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...
The Issue: Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Base for Terumo Advanced Perfusion System 1 Recalled by Terumo...
The Issue: Terumo CVS is implementing field correction activities to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon...
The Issue: Devon Light Glove in procedure kits may have holes/slits compromising...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.