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. 2,595 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,595 in last 12 months

Showing 2302123040 of 52,339 recalls

Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: OR VANTEX 7FR 3L 16CM CVC ECVC6665 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PEDIATRIC PICC INSERTION TRAY CVI4450A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· MAJOR PHARMACEUTICALS

Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS Recalled by MAJOR PHARMACEUTICALS...

The Issue: cGMP deviations: Product was exposed above 50% relative humidity levels...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· Legacy Pharmaceutical Packaging LLC

Recalled Item: Losartan Potassium Tablets Recalled by Legacy Pharmaceutical Packaging LLC...

The Issue: CGMP Deviations: Detection of trace amounts of N-Methylnitrosobutyric acid...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Parsley flakes Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Goldenseal herb c/s Recalled by AmeriHerb International Inc Due to Potential...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Dill weed c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Mullein leaf c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Blessed thistle herb c/s Recalled by AmeriHerb International Inc Due to...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Lemon balm leaf c/s Recalled by AmeriHerb International Inc Due to Potential...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2019· Akorn Inc

Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...

The Issue: Failed impurities/degradation specification: Out of Specification result for...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2019· D.B.P. Distribution

Recalled Item: Titanium 4000 Recalled by D.B.P. Distribution Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: undeclared sildenafil and tadalafil.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A Recalled by Arrow...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC with Chlorag+ard Technology Product Code:PR 45541 HPHNM Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45552 VPS2 Recalled...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow¿ PICC with Chlorag+ard¿ Technology Product Code: PR 45552 HPHNL...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2019· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Product Code: CDA 45052 HPK1A...

The Issue: Lidstock states the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing