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Radiometer America Inc

Radiometer America Inc Recalls

All product recalls associated with Radiometer America Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 33761–33780 of 37665 recalls

Radiometer America Inc: Pump waste tube for blood gas analysis kit. One yellowish...

Tube may break. The firm discovered that the yellowish/white tubes used in their blood gas analyzers (ABL800 Flex Series) were manufactured incorrectly. These tubes have the potential to break off at the black plastic connectors. The breakage may occur during the installation of the tubes or after a short time in use.

FDAJun 22, 2007Nationwide• Radiometer America Inc

Ross Products Division Abbott Laboratories: The Companion ClearStar Pump System, for enteral feeding.

The transducer adapter bracket on the pump could crack or break and potentially result in under delivery of the enteral product.

FDAJun 21, 2007Nationwide• Ross Products Division Abbott Laboratories

Ross Products Division Abbott Laboratories: Embrace Enteral Pump

Continued use of the pump may cause the door pivot point on the back of the pump to crack or break. This will cause the pump to shut down and stop the initiation of enteral feeding.

1...1687 168816891690 1691...1884

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FDAJun 21, 2007Nationwide• Ross Products Division Abbott Laboratories

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6301 Dual Channel Volumetric Infusion Pum...

Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.

FDAJun 21, 2007Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Colleague Single Channel Volumetric Infusion Pumps...

Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.

FDAJun 21, 2007Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6201, SIngle Channel , Volumetric Infusio...

Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.

FDAJun 21, 2007Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter Colleague Triple Channel Volumetric Infusion Pumps...

Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.

FDAJun 21, 2007Nationwide• Baxter Healthcare Corp. Rt.

Polaris Outlaw 525 ATVs (Polaris) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves 2007 model year Polaris "Outlaw 525" ATVs. They are available in black or white.

CPSCJun 20, 2007Nationwide• Polaris Industries Inc., of Medina, Minn.

Baxter Healthcare Corp. Rt.: Baxter Colleague Triple Channel Volumetric Infusion Pumps...

A software anomaly is causing newly upgraded Colleague Triple Channel Infusion Pumps to alarm, display an error code (16:310:867:0002) and stop the infusion. This occurs during user programming with all three channels simultaneously infusing fluids. In reported cases, the pump stopped infusing and both an audible and a visual alarm notification were activated.

FDAJun 20, 2007Nationwide• Baxter Healthcare Corp. Rt.

Applied Composite Technology: VS-1000 Senator Prosthetic Foot, (Categories 5 and 6, siz...

Prosthetic foot device may loosen or separate during use; due to structural inconsistency that may cause a pyramid failure.

FDAJun 20, 2007CA, CO, FL +14 more• Applied Composite Technology

Stationary Gas/Propane Generators (Cummins) – Fire Hazard (2007)

Fire/Burn Risk

The recall involves both commercial and residential model Cummins Power Generation gaseous-fueled stationary generator sets (fueled by propane or natural gas). They have the following model numbers listed on the generator nameplate which is located at the front base of the unit: commercial models GGDB, GGMA/B/C, and GNAA/B/C, and residential models RS15000, RS20000, and RS30000. These units also have serial number A050734102 through L068998479 and "Cummins Power Generation" listed on the generator nameplate.

CPSCJun 19, 2007Nationwide• Cummins Power Generation Inc., of Fridley, Minn.

Instrumentation Laboratory Co.: Instrumentation Laboratory ACL TOP Coagulation Analyzer (...

ACL TOP unit, when in emergency stop may release liquid during recovery sequence and contaminate sample tube.

FDAJun 19, 2007Nationwide• Instrumentation Laboratory Co.

AMS Innovative Center San Jose: American Medical Systems, Inc., (AMS) GreenLight HPS Fibe...

Control knob break: The knob used to finely control the direction of the laser energy may break.

FDAJun 18, 2007Nationwide• AMS Innovative Center San Jose

Smiths Medical MD, Inc.: Smiths CADD Yellow Medication Cassette Reservoir, With cl...

Smith Medical has become aware that an increase in pH may occur with some medications when instilled in the Affected Cassettes. Also, a small number of catheter occlusions have been reported from one customer when these Affected Cassettes have been used for delivering Flolan.

FDAJun 18, 2007PR• Smiths Medical MD, Inc.

Smiths Medical MD, Inc.: Smiths CADD Medication Cassette Reservoir, With clamp and...

FDAJun 18, 2007PR• Smiths Medical MD, Inc.

Spectrum Designs Inc: Spectrum Designs Medical Anatomical I (Silhouette) Malar ...

The product is being recalled because it was discovered the at least one unit in the lot contained a mismatched pair (two rights and no left). Since the lot was produced with equal numbers of pairs, it is assumed that one other unit was packaged with two lefts and no right. This was discovered through a physician complaint.

FDAJun 15, 2007Nationwide• Spectrum Designs Inc

Leflunomide Tablets 10mg (Apotex) - Subpotent Drug (2007)

Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.

Class IIModerate

FDAJun 14, 2007Nationwide• Apotex Corp.

Boston Scientific Target: Boston Scientific Target, Transend EX Soft Tip Guide Wire...

Mislabeling: Product is labeled with the wrong expiration date: 2009-12. The correct expiration date is 2008-12.

FDAJun 14, 2007Nationwide• Boston Scientific Target

Leflunomide Tablets 20mg (Apotex) - Subpotent Drug (2007)

Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.

Class IIModerate

FDAJun 14, 2007Nationwide• Apotex Corp.

Mountain Bicycles with Lefty Forks (Cannondale) – Fork Failure Risk (2007)

The carbon or aluminum bicycle forks were sold on Cannondale mountain bicycle models listed below: Bicycle model code, product Retail price Lefty Speed Carbon SL 2007 Taurine Carbon Team Replica 2007 Scalpel 1 2007 Scalpel Team Replica 2007 Rush Carbon 1 2007 Rush Carbon Team 2007 aftermarket, replacement Lefty Speed Carbon SL forks $5500 $5000 $5500 $6000 $6500 $1400 Lefty Speed DLR 2 (including bonded, 100mm and 80mm) 2007 Rush Carbon 2 (This model also included in the recall for Cranksets - CPSC press release #07-206) 2007 Rush 3 2007 Rush 4 2007 Rush 5 2007 Caffeine 29'er 2007 Scalpel 2 2007 Scalpel 3 2007 Caffeine 1 2007 Caffeine 2 2007 Rush Feminine 1 2007 aftermarket, replacement Lefty Speed (bonded, 100mm and 80mm) DLR 2 2008 Rush Carbon 3 $4500 $2600 $2100 $1700 $1600 $3500 $2600 $2200 $1600 $2000 $950 $3500

CPSCJun 13, 2007Nationwide• Cannondale Bicycle Corp., Bethel, Conn.