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. 2,611 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,611 in last 12 months

Showing 1958119600 of 52,339 recalls

Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Stretch VL Ureteral Stent Set 7FX22-30CM with .035 Sensor UPN: M006185157080...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX STR/150CM Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor UPN: Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Medline Industries Inc

Recalled Item: Custom convenience kits containing Medline brand Sterile Pre-Saturated...

The Issue: Medline identified that there may be a potential for voids in the packaging...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars Pineapple Recalled by Dreyers Grand Ice Cream, Inc. Due...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars Strawberry Recalled by Dreyers Grand Ice Cream, Inc. Due...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars - Variety Pack (contains 24 x 5 oz. units) Strawberry...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Sotalol HCL Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of particulate matter. presence of metal particles.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Sun Pharmaceutical Industries, Inc....

The Issue: Presence of foreign substance: Foreign matter has been identified as latex...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 6, 2020· H J Harkins Company Inc dba Pharma Pac

Recalled Item: Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC...

The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart Pump Kit Recalled by Cardiac Assist, Inc Due to Failure to prime...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15 Recalled...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD Recalled by...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL3 Recalled by...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29 Recalled by...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17 Recalled...

The Issue: Failure to prime due to an assembly error

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Linet Americas

Recalled Item: AVE 2 Birthing Bed - Product Usage: is designated to Recalled by Linet...

The Issue: The UDI on the device label indicates incorrect manufacturer.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing