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. 1,762 recalls have been distributed to Arizona in the last 12 months.
Showing 49461–49480 of 52,339 recalls
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spice Cake Mix Recalled by Jiffy Food Service, LLC Due to Undeclared Allergen
The Issue: Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation...
The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30...
The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Furosemide Injection USP (10 mg/mL) Recalled by Hospira, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ventri Discovery NM 530c Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of an incident which caused a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esteem Programmer Model 6001 Recalled by Envoy Medical Corporation Due to...
The Issue: Envoy Medical is conducting a voluntary correction of a limited number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: There is the potential for solution to leak...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Island Delights Almond Chocolate/Almond Mix Natural Flavor Coconut Haystacks...
The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Island Delights Coconut Haystack Candy Maple Natural Flavor Coconut...
The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Island Delights ALMOND Natural Flavor Coconut Haystacks Recalled by Island...
The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Island Delights COFFEE NATURAL Natural Flavor Coconut Haystacks Recalled by...
The Issue: During a visual inspection from Ohio Dept of Agriculture the firm was...
Recommended Action: Do not consume. Return to store for a refund or discard.