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Andover Healthcare Inc.

Andover Healthcare Inc. Recalls

All product recalls associated with Andover Healthcare Inc..

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Recall Summary

Total Recalls

1000

Past Year

589

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 4961–4980 of 10393 recalls

Co-Flex LF2 3" (Andover) – Packaging Seal Defect (2019)

Incomplete packaging seal of sterile product

Low

FDAJun 19, 2019Nationwide• Andover Healthcare Inc.

Seca Baby Scale Cart (Seca) – Wheel Detachment Risk (2019)

It has been determined that the wheels on the baby scale cart can unexpectedly loosen and in the worst case, detach from the cart completely. If this occurs the cart can become unstable and tip over, potentially leading to the scale falling from the cart. If a baby is left unattended in a cart, the baby could fall off the scale and be subjected to several serious injuries.

Moderate

FDAJun 19, 2019AL, AK, AZ +31 more• Seca Hammer Steindamm 9-25 Hamburg Germany

Co-Flex LF2 4" (Andover) – Packaging Seal Defect (2019)

Incomplete packaging seal of sterile product

Low

FDA

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Jun 19, 2019

Nationwide

• Andover Healthcare Inc.

Co-Flex Med 4" (Andover) – Packaging Seal Defect (2019)

Incomplete packaging seal of sterile product

Low

FDAJun 19, 2019Nationwide• Andover Healthcare Inc.

Co-Flex NL 4" (Andover) – Packaging Seal Defect (2019)

Incomplete packaging seal of sterile product

Low

FDAJun 19, 2019Nationwide• Andover Healthcare Inc.

Co-Flex NL 3" (Andover) – Packaging Seal Defect (2019)

Incomplete packaging seal of sterile product

Low

FDAJun 19, 2019Nationwide• Andover Healthcare Inc.

Co-Flex Med 3" (Andover) – Packaging Seal Defect (2019)

Incomplete packaging seal of sterile product

Low

FDAJun 19, 2019Nationwide• Andover Healthcare Inc.

Ocean Supreme Shrimp Meat – Foreign Object (2019)

The product was recalled because there was a foreign object found inside product packaging.

Class IIModerate

FDAJun 14, 2019CA, IN, OR +1 more• California Shellfish, Inc. dba Hallmark Fisheries

Sevoflurane (Baxter Healthcare) – stability specification failure (2019)

Failed Stability Specifications

Class IIModerate

FDAJun 13, 2019Nationwide• Baxter Healthcare Corporation

Hayward Pool Heater Vent Kits (Hayward) – Carbon Monoxide Risk (2019)

This recall involves the Hayward UHXNEGVT15001 Negative Pressure 6-inch Vent Kit for pool heaters. The vent kit is used exclusively on the Hayward H500FD Gas Heaters. The kit includes the following: one vent pipe adapter for negative pressure galvanized vent pipe, one flue cover plate with hole for vent, #10 sheet metal screws, vent pressure switches, vent pressure switch tubing and vent pressure switch jumper wire. Only Hayward H500FD Gas Heaters that are installed indoors and use 6-inch negative pressure galvanized vent piping are affected by this recall. The name Hayward is stamped into the furnace housing above the water pipes. The model and serial number H500FD is located to the left of the water pipes.

Very High

CPSCJun 12, 2019Nationwide• Hayward Industries Inc, of Nashville, Tenn.

Cat & Jack Lilia Rain Boots – Choking Risk (2019)

Choking Hazard

This recall includes the Cat & Jack "Lilia" toddlers' unicorn rain boots in sizes 5-12. The boots are fuchsia with a white unicorn. The horn on the unicorn's head and mane on the back of the boot are fuchsia, orange, yellow, green, and blue. The model numbers are located on the inside tag of the boot. Model Number Product Name 093-10-4311 Cat & Jack "Lilia" Rain Boots Size 5 093-10-4312 Cat & Jack "Lilia" Rain Boots Size 6 093-10-4313 Cat & Jack "Lilia" Rain Boots Size 7 093-10-4314 Cat & Jack "Lilia" Rain Boots Size 8 093-10-4315 Cat & Jack "Lilia" Rain Boots Size 9 093-10-4316 Cat & Jack "Lilia" Rain Boots Size 10 093-10-4317 Cat & Jack "Lilia" Rain Boots Size 11 093-10-4318 Cat & Jack "Lilia" Rain Boots Size 12

CPSCJun 11, 2019Nationwide• CJCHT Groups LTD., of Hong Kong

HeartStart MRx (Philips) – AC power module failure (2019)

The AC power module may fail at a higher than expected rate. If a fully charged battery is not properly installed, the HeartStart MRx may lose all power and fail to operate. Interruption of monitoring and failure or delay in the delivery of a shock or pacing can occur. A faulty AC Power Module may also fail to charge the battery.

FDAJun 7, 2019Nationwide• Philips North America, LLC

Thor Motor Coach Magnitude (Thor) – wiring problem (2019)

Fire/Burn Risk

Thor Motor Coach (TMC) is recalling certain 2019-2020 Magnitude, Omni motorhomes, models BB35 and BH35. Wires located in the electrical junction box may move around and contact an extra screw that was errantly installed.

NHTSAJun 5, 2019Nationwide• THOR MOTOR COACH

Stratton Pendant Light Fixtures – Injury Risk (2019)

This recall involves the small Stratton pendant light fixtures. The lights are suspended and provide task lighting and general illumination for both consumer and commercial applications. The UPC number is on the light fixture packaging, and the part number is located on a yellow sticker inside of the canopy of the fixture. The recalled small light fixture is 9.2 inches wide, and was sold with a glass shade (clear or smoke color). The recall involves the following item numbers and UPCs: Item Number UPC 700TDSTNPSCB-PAR 884655362979 700TDSTNPSKB-PAR 884655362986 700TDSTNPSCB-LED27 884655362993 700TDSTNPSKB-LED27 884655363006 700TDSTNPSCB-LED30 884655363013 700TDSTNPSKB-LED30 884655363020 700TDSTNPSCY-PAR 884655363099 700TDSTNPSKY-PAR 884655363105 700TDSTNPSCY-LED27 884655363112 700TDSTNPSKY-LED27 884655363129 700TDSTNPSCY-LED30 884655363136 700TDSTNPSKY-LED30 884655363143 700TDSTNPSCB 191963077083 700TDSTNPSCY 191963077090 700TDSTNPSKB 191963077106 700TDSTNPSKY 191963077113

CPSCJun 4, 2019Nationwide• Guangzhou Xiongyi Precision Metalworking Co., Ltd., of China

Jalapeno Peppers (The Fresh Group) – Salmonella risk (2019)

Salmonella

Jalapeno peppers may be contaminated with Salmonella.

Class IHigh

FDAJun 4, 2019IA, MI, MN +2 more• The Fresh Group, Ltd.

Whole Jalapeno (Shelton Farms) – Salmonella contamination (2019)

Salmonella

Class IHigh

FDAJun 3, 2019IN, MI• Shelton Farms dba Shelton's Wholesale Co

REVACLEAR Dialyzer (Baxter) – fiber rupture risk (2019)

There is a potential presence of ruptured dialyzer fibers which may lead to a blood leak during treatment.

FDAMay 31, 2019Nationwide• Baxter Healthcare Corporation

Snickers Cheesecake (Hank's Cheesecakes) – undeclared allergens (2019)

Packaged cheesecakes are distributed with no labels indicating the ingredients or the major food allergens they contain.

Class IIModerate

FDAMay 31, 2019IL, IN, MO• Hank's Cheesecakes, LLC

White Chocolate Raspberry Cheesecake (Hank's Cheesecakes) – undeclared allergens (2019)

Packaged cheesecakes are distributed with no labels indicating the ingredients or the major food allergens they contain.

Class IIModerate

FDAMay 31, 2019IL, IN, MO• Hank's Cheesecakes, LLC

Caramel Macchiato Cheesecake (Hank's Cheesecakes) – undeclared allergens (2019)

Packaged cheesecakes are distributed with no labels indicating the ingredients or the major food allergens they contain.

Class IIModerate

FDAMay 31, 2019IL, IN, MO• Hank's Cheesecakes, LLC