Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 27781–27800 of 52,535 recalls
Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...
The Issue: Dental implants have incorrect item/lot numbers and size on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco RPMI 1640 Medium Recalled by Life Technologies, Corp. Due to It has...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco CTS OpTmizer T Cell Expansion Serum Free Medium Recalled by Life...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBCO CTS AIM V Serum-Free Media (SFM) Recalled by Life Technologies, Corp....
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...
The Issue: Out of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PHYT Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: There is a potential for imprecise results when using the slides. Increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Johnson & Johnson...
The Issue: Software upgrade exhibits failures when executing Daily Alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS-7 Recalled by Konica Minolta Medical Imaging USA, Inc. Due to Panasonic...
The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImagePilot Recalled by Konica Minolta Medical Imaging USA, Inc. Due to...
The Issue: Panasonic has issued a Mandatory Product Safety Notice, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: The firm will be updating the Instructions for Use for the product. Current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: The firm will be updating the Instructions for Use for the product. Current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...
The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...
The Issue: In certain eyepiece configurations the laser shutter may not close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...
The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...
The Issue: Stryker Sustainability Solutions has received an increase in reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivo 65 Recalled by Human Design Medical Llc Due to Some Vivo 65 devices...
The Issue: Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...
The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.