Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,520 in last 12 months

Showing 98819900 of 48,770 recalls

Medical DeviceJanuary 24, 2023· Intuitive Surgical, Inc.

Recalled Item: Patient Side Cart Recalled by Intuitive Surgical, Inc. Due to Preventative...

The Issue: Preventative maintenance data was used to identify instrument Arms, part of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2023· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network...

The Issue: Infusion pump PCs with specific software/network cards/IP addresses can have...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2023· Draeger Medical, Inc.

Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...

The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 23, 2023· Draeger Medical, Inc.

Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...

The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 20, 2023· SUREPULSE MEDICAL LTD

Recalled Item: Surepulse VS Cap Large component of VS Newborn Recalled by SUREPULSE MEDICAL...

The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 20, 2023· SUREPULSE MEDICAL LTD

Recalled Item: Surepulse VS Cap Medium component of VS Newborn Recalled by SUREPULSE...

The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 20, 2023· SUREPULSE MEDICAL LTD

Recalled Item: Surepulse VS Cap Small component of VS Newborn Recalled by SUREPULSE MEDICAL...

The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 20, 2023· SUREPULSE MEDICAL LTD

Recalled Item: Surepulse VS Cap Extra Small component of VS Recalled by SUREPULSE MEDICAL...

The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 20, 2023· SUREPULSE MEDICAL LTD

Recalled Item: Surepulse VS Cap Extra Large component of VS Recalled by SUREPULSE MEDICAL...

The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...

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

Class III — Low RiskOngoing
DrugJanuary 20, 2023· Lupin Pharmaceuticals Inc.

Recalled Item: Clobetasol propionate Cream USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Subpotent Drug: Low assay result observed during long-term stability testing.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 20, 2023· Medtronic Neuromodulation

Recalled Item: SenSight Connector Plug Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic is requesting return of a small number of units of the SenSight...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2023· Coltene Whaledent Inc

Recalled Item: SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of...

The Issue: Screw connection between the turbine head and the push button may loosen and...

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

Class II — Potential Health HazardOngoing
FoodJanuary 18, 2023· Mondelez Global Llc

Recalled Item: Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) Recalled by...

The Issue: Undeclared FD&C Yellow No. 5

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2023· Philips North America

Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due...

The Issue: The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component...

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

Class II — Potential Health HazardOngoing
DrugJanuary 17, 2023· Urban Electric Power

Recalled Item: Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v Recalled by Urban...

The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2023· Urban Electric Power

Recalled Item: Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v) Recalled by Urban Electric...

The Issue: CGMP Deviations: FDA analysis found product to contain acetaldehyde and...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2023· Fisher Scientific Co., LLC

Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...

The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 17, 2023· Fisher Scientific Co., LLC

Recalled Item: Hand Sanitizer Recalled by Fisher Scientific Co., LLC Due to CGMP...

The Issue: CGMP Deviations: Voluntary recall of all hand sanitizer distributed after...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2023· Fujifilm Irvine Scientific, Inc.

Recalled Item: Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) # 9305 Recalled...

The Issue: Due to the detection of oil toxicity in several lots of Oil for Embryo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2023· Hologic, Inc.

Recalled Item: Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D...

The Issue: C-Arm unexpected movement may cause blunt trauma should the tube arm impinge...

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

Class II — Potential Health HazardOngoing