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. 2,544 recalls have been distributed to Arizona in the last 12 months.
Showing 34121–34140 of 52,339 recalls
Recalled Item: FE Maple Recalled by QualiTech, Inc Due to Potential E. coli Contamination
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Green Bell Pepper Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE RedBell Pepper 339 Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Spinach 352 Recalled by QualiTech, Inc Due to Potential E. coli Contamination
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Green Bell Pepper 338 Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Cheddar Cheese Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FI Dry Blueberry / Strawberry Blend Recalled by QualiTech, Inc Due to...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Bacon Recalled by QualiTech, Inc Due to Potential E. coli Contamination
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE RedBell Pepper Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...
The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...
The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.