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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 8601–8620 of 27,655 recalls
Recalled Item: IPELA FHD PTZ TILE KITS with Axis cameras used in Recalled by Natus...
The Issue: Tile kits that allow one to install and situate a video camera within a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veradius Unity Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: Firm discovered that the wireless foot switch can suddenly stop responding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Firm...
The Issue: Firm discovered that the wireless foot switch can suddenly stop responding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Firm...
The Issue: Firm discovered that the wireless foot switch can suddenly stop responding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michels Transport Medium Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARDY DIAGNOSTICS CatScreen Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...
The Issue: The European version of the DiaTrust COVID-19 Ag Rapid Test is not approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Rotaclone Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Product stored incorrectly in temperature controlled setting instead of .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic...
The Issue: ¿2 Microglobulin (B2M) Reagent Lot 211446 Bias with Quality Control and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Bifurcated Recalled by Maquet Cardiovascular, LLC...
The Issue: There is a probable mislabeling of product. A Hemashield Platinum Woven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 -intended for dental...
The Issue: Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Recalled by ROi CPS LLC Due to Kits lacks rubber latex warning label.
The Issue: Kits lacks rubber latex warning label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls Recalled by MEDLINE...
The Issue: Affected product was shipped from the warehouse at room temperature instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: activforce 2 package labeling: Model: Activ5-M R 201-200563 Recalled by...
The Issue: Due to: 1) Manufacturing issue that result in inaccurate force measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medichoice Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmers w/strap Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heel Snuggler Recalled by Philips North America Llc Due to After the device...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.