Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,725 recalls have been distributed to Arizona in the last 12 months.
Showing 13601–13620 of 29,154 recalls
Recalled Item: Dimension¿ Ferritin (FERR) Flex¿ reagent cartridge DM FERR Product Usage:...
The Issue: Negative Bias with Lot EA9227.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Cogent Hemodynamic Monitoring System Recalled by ICU Medical,...
The Issue: Firm identified several software issues through internal testing of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom Receiver Recalled by Dexcom Inc Due to It has been reported that use...
The Issue: It has been reported that use of the mobile receiver with software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an in vitro diagnostic product intended for use Recalled by Randox...
The Issue: Randox Laboratories realigned RX Analyser Series calibration targets by 10%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Pelvic Trainer (MPT) Recalled by Ralston Group Due to The device was...
The Issue: The device was incorrectly listed with the FDA and is therefore considered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...
The Issue: code 7-102 Liquid Sensor Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that BD FACS Sample Prep Assistant (SPA) II and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) III - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II Upgrade - Product Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System Tubing Set kits Product numbers:...
The Issue: The firm received complaints on the saline tubing of Visualase Cooled Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN Recalled by...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.