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. 2,442 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,442 in last 12 months

Showing 3876138780 of 52,339 recalls

FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Cambridge House Balmoral Smoked Salmon Sliced Side - Coastal Recalled by...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: Cambridge House Royal Smoked Salmon Sliced Side Products are packaged...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Wild River Pacific Smoked Salmon 4oz. D-Cut Products are Recalled by The...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Channel Island Atlantic Smoked Salmon Sliced Side - North Recalled by The...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 4, 2015· The Santa Barbara Smokehouse, Inc.

Recalled Item: - Coastal Harbor Oak & Beechwood Smoked Salmon Sliced Side Recalled by The...

The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 4, 2015· Panoramic Rental Corp.

Recalled Item: Panoramic X-ray Model PC-1000 The PC-1000 will enable the user Recalled by...

The Issue: Jackscrew nut part failure potentially leading to device malfunction and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Omnilife Science Inc.

Recalled Item: APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due...

The Issue: The device may have improper screw hole placement due to inaccurate location...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Biomet, Inc.

Recalled Item: A.L.P.S. Foot Locking Calcaneus Plate Recalled by Biomet, Inc. Due to The...

The Issue: The thread location on one of the thread holes is offset from the axis of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Volcano Corporation

Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...

The Issue: During a relabeling procedure at the manufacturing facility, the products...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2015· Volcano Corporation

Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...

The Issue: During a relabeling procedure at the manufacturing facility, the products...

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

Class II — Potential Health HazardOngoing
DrugJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 3, 2015· Baxter Healthcare Corp

Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...

The Issue: Subpotent Drug; out of specification results for heparin raw material

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 3, 2015· Centro Naturista

Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...

The Issue: Multiple dietary supplement regulation violations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...

The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2015· Elite Biomedical Solutions LLC

Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...

The Issue: Administration of inappropriate quantities of fluid can result, with the...

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

Class I — Serious Health HazardOngoing