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. 2,406 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,406 in last 12 months

Showing 5126151280 of 52,339 recalls

FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: Kerry Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2012· Kerry Foods

Recalled Item: KERRY Recalled by Kerry Foods Due to Kerry has decided to voluntarily recall...

The Issue: Kerry has decided to voluntarily recall its lactic acid containing products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Advanced Sterilization Products

Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...

The Issue: The recall was initiated because Advanced Sterilization Products has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...

The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...

The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...

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

Class II — Potential Health HazardOngoing