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. 1,122 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,122 in last 12 months

Showing 9961–9980 of 29,154 recalls

Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Monitoring Set Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Tubing with male luer lock adapter (Component) a. 76 cm Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Gang Cath Lab Set Recalled by Smiths Medical ASD Inc. Due to Specific lots...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: ELI 380 Electrocardiograph Recalled by Welch Allyn Inc Mortara Due to...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Mark 910 LogiCal Recalled by Smiths Medical ASD Inc. Due to Specific lots of...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: HIGH PRESSURE TUBING Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ACE MDI Spacer with Small Mask - Product Usage: designed Recalled by Smiths...

The Issue: The firm became aware via complaints that one lot of ACE MDI Spacers with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD Recalled by Smiths Medical ASD Inc....

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...

The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...

The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Atos Medical AB

Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...

The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Philips North America Llc

Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...

The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...

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

Class II — Potential Health HazardOngoing