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. 2,582 recalls have been distributed to Arizona in the last 12 months.
Showing 27401–27420 of 52,339 recalls
Recalled Item: Intera 1.5T Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5 Model 78104 Product Usage: Indicated for use as a Recalled by Philips...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...
The Issue: The product label has missing information, such as the lot number and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...
The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rectal Catheters Recalled by Teleflex Medical Europe Ltd Due to These...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...
The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a)...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: diet Pepsi Classic Diet Pepsi Taste Recalled by Pepsico Foods International...
The Issue: PepsiCo is recalling Diet Pepsi due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: All Alka-Seltzer Plus¿ packages with a full front panel instant Recalled by...
The Issue: Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...
The Issue: There is an increased risk of false positive Proteus results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...
The Issue: The cap on the vial might be labeled with the incorrect part number but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart (HS1) Onsite/Home AED Recalled by Philips Electronics...
The Issue: An issue with one of the electric components (a resistor) could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx AED. Recalled by Philips Electronics North America...
The Issue: An issue with one of the electric components (a resistor) could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS Xper Flex Cardio Physiomonitoring System Recalled by Invivo...
The Issue: The real-time numeric value for ventricular end-diastolic pressure (EDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...
The Issue: After continuous operation for more than one and a half days, the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...
The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.