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. 2,455 recalls have been distributed to Maine in the last 12 months.
Showing 15541–15560 of 27,655 recalls
Recalled Item: Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with Tri-Staple...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads Recalled by Howmedica Osteonics Corp. Due...
The Issue: The recalling firm has received a higher than expected number of complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...
The Issue: The block used to connect the patient pallet to the couch may be assembled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...
The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...
The Issue: Potential for control line not appearing on the test strip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transferrin is an in vitro diagnostic assay for the quantitative Recalled by...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C3 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G-PIN 2.8BL 3.2PL 60CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Recalled by Abbott Laboratories, Inc Due to An update to the Reagents...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2MM X 510MM COCR THD TIP Recalled by Zimmer Biomet, Inc. Due to The firm...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL TIP GUIDE WIRE 2.0MMX60CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL TIP GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRILL PT GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEAD TIP GD WIRE 3.0MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...
The Issue: The firm is recalling various trauma guide wires due to insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.