Manufacturer
261 recalls in our database name The Anspach Effort, Inc. as the manufacturing or recalling firm.
Of the 261 recalls from The Anspach Effort, Inc. we have scored against our rubric, 1 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (2%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
The Anspach Effort, Inc. is recalling 302 Synthes Small Electric Drive units because they may malfunction or start unintentionally.
The Anspach Effort, Inc. is recalling 599 Synthes Small Electric Drive units because they may malfunction, fail to operate, or start unintentionally.
The Anspach Effort, Inc. is recalling Synthes Battery Power Line II Oscillator Model 530.710 units because the saw head may separate from the drive unit or come loose.
The Anspach Effort, Inc. is recalling 246 units of the 4mm Diamond Ball dissection tool because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 70 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.
The Anspach Effort, Inc. is recalling 70 G1 dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 79 Anspach 5MM Fluted Ball dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 99 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual usage, potentially resulting in greater exposure than specified.
The Anspach Effort, Inc. is recalling 72 Anspach Extra Coarse Diamond Ball tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure.
The Anspach Effort, Inc. is recalling 138 fluted drum dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 177 fluted drum dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 70 Anspach 5MM Diamond Ball dissection tools because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 110 fluted barrel dissection tools because the labeled shaft exposure may be inconsistent with actual usage.
The Anspach Effort, Inc. is recalling 189 Anspach 7MM Fluted Acorn dissection tools because the specified shaft exposure on the label may not be consistent with all listed attachments.
The Anspach Effort, Inc. is recalling 69 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure.
The Anspach Effort, Inc. is recalling 75 Anspach 7mm Extra Coarse Diamond Ball dissection tools because the specified shaft exposure may be inconsistent with the labeled attachments.
The Anspach Effort, Inc. is recalling 686 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 796 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.
The Anspach Effort, Inc. is recalling 88 G1 dissection tools because the labeled shaft exposure may be inconsistent with actual use, potentially resulting in greater exposure than specified.
The Anspach Effort, Inc. is recalling 65 Fluted Drum dissection tools because the specified shaft exposure may be inconsistent with attachments, potentially resulting in greater exposure.
The Anspach Effort, Inc. is recalling 88 Extra Coarse Diamond Drums because the shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 110 Anspach Fluted Barrel dissection tools because the specified shaft exposure may be inconsistent with attachments, potentially resulting in greater exposure.
The Anspach Effort, Inc. is recalling 95 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.
The Anspach Effort, Inc. is recalling 353 Fluted Ball dissection tools because the labeled shaft exposure may be inconsistent with actual usage.
The Anspach Effort, Inc. is recalling 103 G1 dissection tools because the specified shaft exposure may be greater than labeled when used with certain attachments.