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Shenzhen Baihang Recalls VEEKTOMX Mini Power Banks, Due to Fire and Burn Hazards; Sold on Amazon
CPSCGeneral Alert

Shenzhen Baihang Recalls VEEKTOMX Mini Power Banks, Due to Fire and Burn Hazards; Sold on Amazon

The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.

Apr 9, 2026
Safety AlertCanadaHealth Canada

Rexall and Pro-Line chemical products recalled due to lack of child-resistant packaging

Consumer product safety
Health CanadaGeneral Alert

Rexall and Pro-Line chemical products recalled due to lack of child-resistant packaging

Labelling and packaging

Apr 9, 2026Consumer product safety
Vehicle RecallUSNHTSA

Honda (American Honda Motor Co.) - Air Bags May Deploy Unexpectedly

Honda (American Honda Motor Co.)
NHTSAAIR BAGS

Honda (American Honda Motor Co.) - Air Bags May Deploy Unexpectedly

Air bags that deploy unexpectedly can increase the risk of injury.

Apr 9, 2026Honda (American Honda Motor Co.)
Medical DeviceUSFDA Devices

BD Kiestra" ReadA; Catalog No.: 446948.

BD KIESTRA LAB AUTOMATION
FDA DevicesClass II

BD Kiestra" ReadA; Catalog No.: 446948.

In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this occurred, there was potential for delays in plate retrieval from the incubator while connectivity was restored. This issue was intermittent and did not affect test results, performance of the assay, or sample integrity.

Apr 8, 2026BD KIESTRA LAB AUTOMATION
Medical DeviceUSFDA Devices

Burlington Medical, Protective Sleeves.

Burlington Medical, LLC
FDA DevicesClass II

Burlington Medical, Protective Sleeves.

Potential for attenuation degradation over time, decreasing the lifespan.

Apr 8, 2026Burlington Medical, LLC
Food & BeverageUSFDA Food

Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap.

The Maros Group, LLC
FDA FoodClass II

Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap.

Undeclared milk.

Apr 8, 2026The Maros Group, LLC
Medical DeviceUSFDA Devices

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

Reflexion Medical, Inc.
FDA DevicesClass II

RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00

Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the initial localization scan are not carried through to treatment delivery leading to the treatment plan dose being delivered to the incorrect location, potentially a displacement of 5mm or higher, with a 10% to 20% underdose.

Apr 8, 2026Reflexion Medical, Inc.
Medical DeviceUSFDA Devices

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

Civco Medical Instruments Co. Inc.
FDA DevicesClass II

eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

Apr 8, 2026Civco Medical Instruments Co. Inc.
Medical DeviceUSFDA Devices

eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152

Civco Medical Instruments Co. Inc.
FDA DevicesClass II

eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

Apr 8, 2026Civco Medical Instruments Co. Inc.
Medical DeviceUSFDA Devices

eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151

Civco Medical Instruments Co. Inc.
FDA DevicesClass II

eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

Apr 8, 2026Civco Medical Instruments Co. Inc.
Medical DeviceUSFDA Devices

ALLURA Xper FD10F; System Code: 722002;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

ALLURA Xper FD10F; System Code: 722002;

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Apr 8, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PharmaceuticalUSFDA Drugs

Prazosin Hydrochloride Capsules, USP, 2mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-067-11.

Appco Pharma LLC
FDA DrugsClass II

Prazosin Hydrochloride Capsules, USP, 2mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-067-11.

cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.

Apr 8, 2026Appco Pharma LLC
Medical DeviceUSFDA Devices

MiniMed 530G Insulin Pump (MMT-551, MMT-751)

Medtronic MiniMed, Inc.
FDA DevicesClass II

MiniMed 530G Insulin Pump (MMT-551, MMT-751)

All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.

Apr 8, 2026Medtronic MiniMed, Inc.
Medical DeviceUSFDA Devices

Allura Xper FD20/10; System Code: 722029;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Allura Xper FD20/10; System Code: 722029;

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Apr 8, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Burlington Medical, Frontal Aprons

Burlington Medical, LLC
FDA DevicesClass II

Burlington Medical, Frontal Aprons

Potential for attenuation degradation over time, decreasing the lifespan.

Apr 8, 2026Burlington Medical, LLC
Medical DeviceUSFDA Devices

Allura Xper FD10C; System Code: 722001;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Allura Xper FD10C; System Code: 722001;

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Apr 8, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Burlington Medical, Leg Wraps.

Burlington Medical, LLC
FDA DevicesClass II

Burlington Medical, Leg Wraps.

Potential for attenuation degradation over time, decreasing the lifespan.

Apr 8, 2026Burlington Medical, LLC
Food & BeverageUSFDA Food

Mama Rose's Prickly Pear Salad Dressing. 12 oz (340 g) glass bottle with gold cap.

The Maros Group, LLC
FDA FoodClass II

Mama Rose's Prickly Pear Salad Dressing. 12 oz (340 g) glass bottle with gold cap.

Undeclared sulfites.

Apr 8, 2026The Maros Group, LLC
Medical DeviceUSFDA Devices

Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Apr 8, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
PharmaceuticalUSFDA Drugs

Dry Eye Relief Eye Drops, (glycerin 0.2%, hypromellose 0.2% and polyethylene glycol 400 1%) 0.5 FL OZ (15 mL) bottles; a) GERI CARE, Distributed by: Gericare Pharmaceuticals Corp., Lakewood, NJ 08701, NDC 57896-181-05; b) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 36100 3; c) Rite Aid, DISTRIBUTEDBY: RITE AID, Camp Hill, PA 17011, NDC 11822-1067-2; d) LEADER DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0502-1; e) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC 0 93351 01156 6; f) H-E-B, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43741 2; g) Foster & Thrive, Distributed by: McKesson Corp., via Strategic Sourcing Services LLC, Memphis, TN 38141, www.fosterandthrive.com, NDC 70677-1158-1; h) meijer, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544, www.meijer.com, NDC 41250-718-01; i) DG health Sterile, DISTRIBUTED BY OLD EAST MAIN CO., GOODLETTSVILLE, TN 37072, UPC 0 95072 02656 0; j) Harris Teeter, Eye Drops, Artificial Tears, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATHEWS, NC 28105, UPC 0 72036 71303 2; k) exchange select, Manufactured for your Military Exchanges by: KC Pharmaceuticals, Inc., Pomona, CA 91768, UPC 6 14299 05620 6; l) Good Neighbor Pharmacy, Distributed By AmerisourceBergen, Conshohocken, PA 19428, NDC 46122-605-05

K.C. Pharmaceuticals, Inc
FDA DrugsClass II

Dry Eye Relief Eye Drops, (glycerin 0.2%, hypromellose 0.2% and polyethylene glycol 400 1%) 0.5 FL OZ (15 mL) bottles; a) GERI CARE, Distributed by: Gericare Pharmaceuticals Corp., Lakewood, NJ 08701, NDC 57896-181-05; b) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 36100 3; c) Rite Aid, DISTRIBUTEDBY: RITE AID, Camp Hill, PA 17011, NDC 11822-1067-2; d) LEADER DISTRIBUTED BY CARDINAL HEALTH, DUBLIN, OHIO 43017, www.myleader.com, NDC 70000-0502-1; e) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC 0 93351 01156 6; f) H-E-B, MADE WITH PRIDE & CARE FOR H-E-B, SAN ANTONIO, TX 78204, UPC 0 41220 43741 2; g) Foster & Thrive, Distributed by: McKesson Corp., via Strategic Sourcing Services LLC, Memphis, TN 38141, www.fosterandthrive.com, NDC 70677-1158-1; h) meijer, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544, www.meijer.com, NDC 41250-718-01; i) DG health Sterile, DISTRIBUTED BY OLD EAST MAIN CO., GOODLETTSVILLE, TN 37072, UPC 0 95072 02656 0; j) Harris Teeter, Eye Drops, Artificial Tears, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATHEWS, NC 28105, UPC 0 72036 71303 2; k) exchange select, Manufactured for your Military Exchanges by: KC Pharmaceuticals, Inc., Pomona, CA 91768, UPC 6 14299 05620 6; l) Good Neighbor Pharmacy, Distributed By AmerisourceBergen, Conshohocken, PA 19428, NDC 46122-605-05

Lack of Assurance of Sterility

Apr 8, 2026K.C. Pharmaceuticals, Inc
Food & BeverageUSFDA Food

MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237 UPC: 6912449124312

Super World Trading Inc.
FDA FoodClass III

MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237 UPC: 6912449124312

Products contain cyclamates (banned sweetener)

Apr 8, 2026Super World Trading Inc.
PharmaceuticalUSFDA Drugs

EYE DROPS Advanced Relief, (dextran 70 0.1%, polyethylene glycol 400 1% and tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) bottles, Sterile; a) Walgreens, DISTRIBUTED BY: WALGREEN CO., DEERFIELD, IL 60015; UPC 3 11917 20074 3; b) Kroger, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202; c) CVS Health, Distributed by :CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 43544 1; d) QC-Quality Choice, Distributed by: CDMA, Inc., Novi, MI 48375, NDC 83324-191-14; e) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC 0 93351 01155 9; f) Foster & Thrive, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141, NDC 70677-1158-1; g) GoodSense, Distributed By: Perrigo Direct Inc., Peachtree City, GA 30269, www.PerrigoDirect.com, NDC 50804-130-01; h) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 03641 3; I) DG health Sterile, DISTRIBUTED BY OLD EAST MAIN CO., 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072, UPC 0 95072 02556 3; j) Fast Acting, CODE RED Eye Drops, Sterile, Distributed by: 4 Trees, LLC, NDC 83817-963-01.

K.C. Pharmaceuticals, Inc
FDA DrugsClass II

EYE DROPS Advanced Relief, (dextran 70 0.1%, polyethylene glycol 400 1% and tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) bottles, Sterile; a) Walgreens, DISTRIBUTED BY: WALGREEN CO., DEERFIELD, IL 60015; UPC 3 11917 20074 3; b) Kroger, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202; c) CVS Health, Distributed by :CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 43544 1; d) QC-Quality Choice, Distributed by: CDMA, Inc., Novi, MI 48375, NDC 83324-191-14; e) Discount drug mart, Discount Drug Mart Food Fair, Medina, OH 44256, UPC 0 93351 01155 9; f) Foster & Thrive, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141, NDC 70677-1158-1; g) GoodSense, Distributed By: Perrigo Direct Inc., Peachtree City, GA 30269, www.PerrigoDirect.com, NDC 50804-130-01; h) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELKGROVE VILLAGE, IL 60007, UPC 0 36800 03641 3; I) DG health Sterile, DISTRIBUTED BY OLD EAST MAIN CO., 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072, UPC 0 95072 02556 3; j) Fast Acting, CODE RED Eye Drops, Sterile, Distributed by: 4 Trees, LLC, NDC 83817-963-01.

Lack of Assurance of Sterility

Apr 8, 2026K.C. Pharmaceuticals, Inc
Food & BeverageUSFDA Food

Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emulsion stabilizer [sodium caseinate, mono- and diglycerides fatty acid esters, sucrose fatty acid esters]; Storage Condition: Room temperature; Manufactured in: Hainan, China; imported By: HK HEYTEA FOOD AND BEVERAGE MANAGEMENT LIMITED; For catering establishment; UPC: 673367992785

HEYTEA USA INC
FDA FoodClass II

Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emulsion stabilizer [sodium caseinate, mono- and diglycerides fatty acid esters, sucrose fatty acid esters]; Storage Condition: Room temperature; Manufactured in: Hainan, China; imported By: HK HEYTEA FOOD AND BEVERAGE MANAGEMENT LIMITED; For catering establishment; UPC: 673367992785

Product contains undeclared milk.

Apr 8, 2026HEYTEA USA INC
Medical DeviceUSFDA Devices

2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.

Synthes (USA) Products LLC
FDA DevicesClass II

2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.

A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.

Apr 8, 2026Synthes (USA) Products LLC
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