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. 1,012 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,012 in last 12 months

Showing 34281–34300 of 52,339 recalls

Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000V 90" 20 Drop IV Admin Set w/ Needlefree Y-Site. Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-120F with 1.2 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000VF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· Hill-Rom, Inc.

Recalled Item: Volker 2080 Recalled by Hill-Rom, Inc. Due to The current construction of...

The Issue: The current construction of the side rail latch may not be able to support...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...

The Issue: The pouch label was missing the use by date (UBD) of 2018-04.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Richard-Allan Scientific Company

Recalled Item: Richard Allan Scientific 10% Neutral Buffered Formalin Recalled by...

The Issue: potential contamination with potassium hydroxide may have an impact when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Biomet Microfixation, LLC

Recalled Item: Hard Tissue Replacement (HTR) Implant Recalled by Biomet Microfixation, LLC...

The Issue: Potential sterility deficiency.

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

Class II — Potential Health HazardOngoing
DrugJune 13, 2016· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Methylprednisolone Tablets Recalled by Jubilant Cadista Pharmaceuticals,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration...

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

Class III — Low RiskOngoing
Refund
DrugJune 13, 2016· Sagent Pharmaceuticals Inc

Recalled Item: Oxacillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Presence of Particulate Matter; The firm received two product complaints for...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Graham Crumbs Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Animals Crackers Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Gripz Chips D 325 ct Bulk Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund